Name: rs11365534
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs11365534

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:35740898-35740917 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₆ / del(T)₅ / del(T)₄ / delT…
del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₄
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.1927 (1263/6554, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ARMC12 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6554	TTTTTTTTTTTTTTTTTTTT=0.7530	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.1927, TTTTTTTTTTTTTTTTTTTTT=0.0482, TTTTTTTTTTTTTTTTTTTTTT=0.0034, TTTTTTTTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.689644	0.068931	0.241426	32
European	Sub	6084	TTTTTTTTTTTTTTTTTTTT=0.7349	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.2071, TTTTTTTTTTTTTTTTTTTTT=0.0514, TTTTTTTTTTTTTTTTTTTTTT=0.0036, TTTTTTTTTTTTTTTTTTTTTTT=0.0021, TTTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.663991	0.074425	0.261583	32
African	Sub	146	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	10	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	136	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	26	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	24	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	26	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	178	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	12	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	82	TTTTTTTTTTTTTTTTTTTT=0.93	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.948718	0.025641	0.025641	10

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6554	(T)₂₀=0.7530	del(T)₆=0.0000, del(T)₅=0.0000, delTT=0.0000, delT=0.1927, dupT=0.0482, dupTT=0.0034, dupTTT=0.0020, dup(T)₄=0.0005, dup(T)₅=0.0000, dup(T)₆=0.0003, dup(T)₇=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	European	Sub	6084	(T)₂₀=0.7349	del(T)₆=0.0000, del(T)₅=0.0000, delTT=0.0000, delT=0.2071, dupT=0.0514, dupTT=0.0036, dupTTT=0.0021, dup(T)₄=0.0005, dup(T)₅=0.0000, dup(T)₆=0.0003, dup(T)₇=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	178	(T)₂₀=1.000	del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	African	Sub	146	(T)₂₀=1.000	del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Other	Sub	82	(T)₂₀=0.93	del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.04, dupT=0.04, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	26	(T)₂₀=1.00	del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Asian	Sub	26	(T)₂₀=1.00	del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(T)₂₀=1.00	del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 6	NC_000006.12:g.35740912_35740917del
GRCh38.p14 chr 6	NC_000006.12:g.35740913_35740917del
GRCh38.p14 chr 6	NC_000006.12:g.35740914_35740917del
GRCh38.p14 chr 6	NC_000006.12:g.35740915_35740917del
GRCh38.p14 chr 6	NC_000006.12:g.35740916_35740917del
GRCh38.p14 chr 6	NC_000006.12:g.35740917del
GRCh38.p14 chr 6	NC_000006.12:g.35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740916_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740915_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740914_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740913_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740912_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740911_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740910_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740909_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740908_35740917dup
GRCh38.p14 chr 6	NC_000006.12:g.35740904_35740917dup
GRCh37.p13 chr 6	NC_000006.11:g.35708689_35708694del
GRCh37.p13 chr 6	NC_000006.11:g.35708690_35708694del
GRCh37.p13 chr 6	NC_000006.11:g.35708691_35708694del
GRCh37.p13 chr 6	NC_000006.11:g.35708692_35708694del
GRCh37.p13 chr 6	NC_000006.11:g.35708693_35708694del
GRCh37.p13 chr 6	NC_000006.11:g.35708694del
GRCh37.p13 chr 6	NC_000006.11:g.35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708693_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708692_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708691_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708690_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708689_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708688_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708687_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708686_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708685_35708694dup
GRCh37.p13 chr 6	NC_000006.11:g.35708681_35708694dup
ARMC12 RefSeqGene	NG_052798.1:g.12187_12192del
ARMC12 RefSeqGene	NG_052798.1:g.12188_12192del
ARMC12 RefSeqGene	NG_052798.1:g.12189_12192del
ARMC12 RefSeqGene	NG_052798.1:g.12190_12192del
ARMC12 RefSeqGene	NG_052798.1:g.12191_12192del
ARMC12 RefSeqGene	NG_052798.1:g.12192del
ARMC12 RefSeqGene	NG_052798.1:g.12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12191_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12190_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12189_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12188_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12187_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12186_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12185_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12184_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12183_12192dup
ARMC12 RefSeqGene	NG_052798.1:g.12179_12192dup

Gene: ARMC12, armadillo repeat containing 12 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ARMC12 transcript variant 2	NM_001286574.2:c.444+2394… NM_001286574.2:c.444+2394_444+2399del	N/A	Intron Variant
ARMC12 transcript variant 3	NM_001286576.2:c.444+2394… NM_001286576.2:c.444+2394_444+2399del	N/A	Intron Variant
ARMC12 transcript variant 1	NM_145028.5:c.525+2394_52… NM_145028.5:c.525+2394_525+2399del	N/A	Intron Variant
ARMC12 transcript variant X2	XM_011514381.3:c.330+2394… XM_011514381.3:c.330+2394_330+2399del	N/A	Intron Variant
ARMC12 transcript variant X3	XM_011514382.3:c.183+2394… XM_011514382.3:c.183+2394_183+2399del	N/A	Intron Variant
ARMC12 transcript variant X4	XM_017010435.3:c.525+2394… XM_017010435.3:c.525+2394_525+2399del	N/A	Intron Variant
ARMC12 transcript variant X5	XM_047418343.1:c.525+2394… XM_047418343.1:c.525+2394_525+2399del	N/A	Intron Variant
ARMC12 transcript variant X6	XM_047418344.1:c.525+2394… XM_047418344.1:c.525+2394_525+2399del	N/A	Intron Variant
ARMC12 transcript variant X7	XM_047418345.1:c.525+2394… XM_047418345.1:c.525+2394_525+2399del	N/A	Intron Variant
ARMC12 transcript variant X8	XM_047418346.1:c.525+2394… XM_047418346.1:c.525+2394_525+2399del	N/A	Intron Variant
ARMC12 transcript variant X9	XM_047418347.1:c.444+2394… XM_047418347.1:c.444+2394_444+2399del	N/A	Intron Variant
ARMC12 transcript variant X1	XM_047418348.1:c.444+2394… XM_047418348.1:c.444+2394_444+2399del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₀=	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₄
GRCh38.p14 chr 6	NC_000006.12:g.35740898_35740917=	NC_000006.12:g.35740912_35740917del	NC_000006.12:g.35740913_35740917del	NC_000006.12:g.35740914_35740917del	NC_000006.12:g.35740915_35740917del	NC_000006.12:g.35740916_35740917del	NC_000006.12:g.35740917del	NC_000006.12:g.35740917dup	NC_000006.12:g.35740916_35740917dup	NC_000006.12:g.35740915_35740917dup	NC_000006.12:g.35740914_35740917dup	NC_000006.12:g.35740913_35740917dup	NC_000006.12:g.35740912_35740917dup	NC_000006.12:g.35740911_35740917dup	NC_000006.12:g.35740910_35740917dup	NC_000006.12:g.35740909_35740917dup	NC_000006.12:g.35740908_35740917dup	NC_000006.12:g.35740904_35740917dup
GRCh37.p13 chr 6	NC_000006.11:g.35708675_35708694=	NC_000006.11:g.35708689_35708694del	NC_000006.11:g.35708690_35708694del	NC_000006.11:g.35708691_35708694del	NC_000006.11:g.35708692_35708694del	NC_000006.11:g.35708693_35708694del	NC_000006.11:g.35708694del	NC_000006.11:g.35708694dup	NC_000006.11:g.35708693_35708694dup	NC_000006.11:g.35708692_35708694dup	NC_000006.11:g.35708691_35708694dup	NC_000006.11:g.35708690_35708694dup	NC_000006.11:g.35708689_35708694dup	NC_000006.11:g.35708688_35708694dup	NC_000006.11:g.35708687_35708694dup	NC_000006.11:g.35708686_35708694dup	NC_000006.11:g.35708685_35708694dup	NC_000006.11:g.35708681_35708694dup
ARMC12 RefSeqGene	NG_052798.1:g.12173_12192=	NG_052798.1:g.12187_12192del	NG_052798.1:g.12188_12192del	NG_052798.1:g.12189_12192del	NG_052798.1:g.12190_12192del	NG_052798.1:g.12191_12192del	NG_052798.1:g.12192del	NG_052798.1:g.12192dup	NG_052798.1:g.12191_12192dup	NG_052798.1:g.12190_12192dup	NG_052798.1:g.12189_12192dup	NG_052798.1:g.12188_12192dup	NG_052798.1:g.12187_12192dup	NG_052798.1:g.12186_12192dup	NG_052798.1:g.12185_12192dup	NG_052798.1:g.12184_12192dup	NG_052798.1:g.12183_12192dup	NG_052798.1:g.12179_12192dup
ARMC12 transcript variant 2	NM_001286574.2:c.444+2380=	NM_001286574.2:c.444+2394_444+2399del	NM_001286574.2:c.444+2395_444+2399del	NM_001286574.2:c.444+2396_444+2399del	NM_001286574.2:c.444+2397_444+2399del	NM_001286574.2:c.444+2398_444+2399del	NM_001286574.2:c.444+2399del	NM_001286574.2:c.444+2399dup	NM_001286574.2:c.444+2398_444+2399dup	NM_001286574.2:c.444+2397_444+2399dup	NM_001286574.2:c.444+2396_444+2399dup	NM_001286574.2:c.444+2395_444+2399dup	NM_001286574.2:c.444+2394_444+2399dup	NM_001286574.2:c.444+2393_444+2399dup	NM_001286574.2:c.444+2392_444+2399dup	NM_001286574.2:c.444+2391_444+2399dup	NM_001286574.2:c.444+2390_444+2399dup	NM_001286574.2:c.444+2386_444+2399dup
ARMC12 transcript variant 3	NM_001286576.2:c.444+2380=	NM_001286576.2:c.444+2394_444+2399del	NM_001286576.2:c.444+2395_444+2399del	NM_001286576.2:c.444+2396_444+2399del	NM_001286576.2:c.444+2397_444+2399del	NM_001286576.2:c.444+2398_444+2399del	NM_001286576.2:c.444+2399del	NM_001286576.2:c.444+2399dup	NM_001286576.2:c.444+2398_444+2399dup	NM_001286576.2:c.444+2397_444+2399dup	NM_001286576.2:c.444+2396_444+2399dup	NM_001286576.2:c.444+2395_444+2399dup	NM_001286576.2:c.444+2394_444+2399dup	NM_001286576.2:c.444+2393_444+2399dup	NM_001286576.2:c.444+2392_444+2399dup	NM_001286576.2:c.444+2391_444+2399dup	NM_001286576.2:c.444+2390_444+2399dup	NM_001286576.2:c.444+2386_444+2399dup
ARMC12 transcript	NM_145028.3:c.525+2380=	NM_145028.3:c.525+2394_525+2399del	NM_145028.3:c.525+2395_525+2399del	NM_145028.3:c.525+2396_525+2399del	NM_145028.3:c.525+2397_525+2399del	NM_145028.3:c.525+2398_525+2399del	NM_145028.3:c.525+2399del	NM_145028.3:c.525+2399dup	NM_145028.3:c.525+2398_525+2399dup	NM_145028.3:c.525+2397_525+2399dup	NM_145028.3:c.525+2396_525+2399dup	NM_145028.3:c.525+2395_525+2399dup	NM_145028.3:c.525+2394_525+2399dup	NM_145028.3:c.525+2393_525+2399dup	NM_145028.3:c.525+2392_525+2399dup	NM_145028.3:c.525+2391_525+2399dup	NM_145028.3:c.525+2390_525+2399dup	NM_145028.3:c.525+2386_525+2399dup
ARMC12 transcript variant 1	NM_145028.5:c.525+2380=	NM_145028.5:c.525+2394_525+2399del	NM_145028.5:c.525+2395_525+2399del	NM_145028.5:c.525+2396_525+2399del	NM_145028.5:c.525+2397_525+2399del	NM_145028.5:c.525+2398_525+2399del	NM_145028.5:c.525+2399del	NM_145028.5:c.525+2399dup	NM_145028.5:c.525+2398_525+2399dup	NM_145028.5:c.525+2397_525+2399dup	NM_145028.5:c.525+2396_525+2399dup	NM_145028.5:c.525+2395_525+2399dup	NM_145028.5:c.525+2394_525+2399dup	NM_145028.5:c.525+2393_525+2399dup	NM_145028.5:c.525+2392_525+2399dup	NM_145028.5:c.525+2391_525+2399dup	NM_145028.5:c.525+2390_525+2399dup	NM_145028.5:c.525+2386_525+2399dup
ARMC12 transcript variant X1	XM_005248919.1:c.525+2380=	XM_005248919.1:c.525+2394_525+2399del	XM_005248919.1:c.525+2395_525+2399del	XM_005248919.1:c.525+2396_525+2399del	XM_005248919.1:c.525+2397_525+2399del	XM_005248919.1:c.525+2398_525+2399del	XM_005248919.1:c.525+2399del	XM_005248919.1:c.525+2399dup	XM_005248919.1:c.525+2398_525+2399dup	XM_005248919.1:c.525+2397_525+2399dup	XM_005248919.1:c.525+2396_525+2399dup	XM_005248919.1:c.525+2395_525+2399dup	XM_005248919.1:c.525+2394_525+2399dup	XM_005248919.1:c.525+2393_525+2399dup	XM_005248919.1:c.525+2392_525+2399dup	XM_005248919.1:c.525+2391_525+2399dup	XM_005248919.1:c.525+2390_525+2399dup	XM_005248919.1:c.525+2386_525+2399dup
ARMC12 transcript variant X2	XM_005248920.1:c.525+2380=	XM_005248920.1:c.525+2394_525+2399del	XM_005248920.1:c.525+2395_525+2399del	XM_005248920.1:c.525+2396_525+2399del	XM_005248920.1:c.525+2397_525+2399del	XM_005248920.1:c.525+2398_525+2399del	XM_005248920.1:c.525+2399del	XM_005248920.1:c.525+2399dup	XM_005248920.1:c.525+2398_525+2399dup	XM_005248920.1:c.525+2397_525+2399dup	XM_005248920.1:c.525+2396_525+2399dup	XM_005248920.1:c.525+2395_525+2399dup	XM_005248920.1:c.525+2394_525+2399dup	XM_005248920.1:c.525+2393_525+2399dup	XM_005248920.1:c.525+2392_525+2399dup	XM_005248920.1:c.525+2391_525+2399dup	XM_005248920.1:c.525+2390_525+2399dup	XM_005248920.1:c.525+2386_525+2399dup
ARMC12 transcript variant X3	XM_005248921.1:c.444+2380=	XM_005248921.1:c.444+2394_444+2399del	XM_005248921.1:c.444+2395_444+2399del	XM_005248921.1:c.444+2396_444+2399del	XM_005248921.1:c.444+2397_444+2399del	XM_005248921.1:c.444+2398_444+2399del	XM_005248921.1:c.444+2399del	XM_005248921.1:c.444+2399dup	XM_005248921.1:c.444+2398_444+2399dup	XM_005248921.1:c.444+2397_444+2399dup	XM_005248921.1:c.444+2396_444+2399dup	XM_005248921.1:c.444+2395_444+2399dup	XM_005248921.1:c.444+2394_444+2399dup	XM_005248921.1:c.444+2393_444+2399dup	XM_005248921.1:c.444+2392_444+2399dup	XM_005248921.1:c.444+2391_444+2399dup	XM_005248921.1:c.444+2390_444+2399dup	XM_005248921.1:c.444+2386_444+2399dup
ARMC12 transcript variant X4	XM_005248922.1:c.444+2380=	XM_005248922.1:c.444+2394_444+2399del	XM_005248922.1:c.444+2395_444+2399del	XM_005248922.1:c.444+2396_444+2399del	XM_005248922.1:c.444+2397_444+2399del	XM_005248922.1:c.444+2398_444+2399del	XM_005248922.1:c.444+2399del	XM_005248922.1:c.444+2399dup	XM_005248922.1:c.444+2398_444+2399dup	XM_005248922.1:c.444+2397_444+2399dup	XM_005248922.1:c.444+2396_444+2399dup	XM_005248922.1:c.444+2395_444+2399dup	XM_005248922.1:c.444+2394_444+2399dup	XM_005248922.1:c.444+2393_444+2399dup	XM_005248922.1:c.444+2392_444+2399dup	XM_005248922.1:c.444+2391_444+2399dup	XM_005248922.1:c.444+2390_444+2399dup	XM_005248922.1:c.444+2386_444+2399dup
ARMC12 transcript variant X2	XM_011514381.3:c.330+2380=	XM_011514381.3:c.330+2394_330+2399del	XM_011514381.3:c.330+2395_330+2399del	XM_011514381.3:c.330+2396_330+2399del	XM_011514381.3:c.330+2397_330+2399del	XM_011514381.3:c.330+2398_330+2399del	XM_011514381.3:c.330+2399del	XM_011514381.3:c.330+2399dup	XM_011514381.3:c.330+2398_330+2399dup	XM_011514381.3:c.330+2397_330+2399dup	XM_011514381.3:c.330+2396_330+2399dup	XM_011514381.3:c.330+2395_330+2399dup	XM_011514381.3:c.330+2394_330+2399dup	XM_011514381.3:c.330+2393_330+2399dup	XM_011514381.3:c.330+2392_330+2399dup	XM_011514381.3:c.330+2391_330+2399dup	XM_011514381.3:c.330+2390_330+2399dup	XM_011514381.3:c.330+2386_330+2399dup
ARMC12 transcript variant X3	XM_011514382.3:c.183+2380=	XM_011514382.3:c.183+2394_183+2399del	XM_011514382.3:c.183+2395_183+2399del	XM_011514382.3:c.183+2396_183+2399del	XM_011514382.3:c.183+2397_183+2399del	XM_011514382.3:c.183+2398_183+2399del	XM_011514382.3:c.183+2399del	XM_011514382.3:c.183+2399dup	XM_011514382.3:c.183+2398_183+2399dup	XM_011514382.3:c.183+2397_183+2399dup	XM_011514382.3:c.183+2396_183+2399dup	XM_011514382.3:c.183+2395_183+2399dup	XM_011514382.3:c.183+2394_183+2399dup	XM_011514382.3:c.183+2393_183+2399dup	XM_011514382.3:c.183+2392_183+2399dup	XM_011514382.3:c.183+2391_183+2399dup	XM_011514382.3:c.183+2390_183+2399dup	XM_011514382.3:c.183+2386_183+2399dup
ARMC12 transcript variant X4	XM_017010435.3:c.525+2380=	XM_017010435.3:c.525+2394_525+2399del	XM_017010435.3:c.525+2395_525+2399del	XM_017010435.3:c.525+2396_525+2399del	XM_017010435.3:c.525+2397_525+2399del	XM_017010435.3:c.525+2398_525+2399del	XM_017010435.3:c.525+2399del	XM_017010435.3:c.525+2399dup	XM_017010435.3:c.525+2398_525+2399dup	XM_017010435.3:c.525+2397_525+2399dup	XM_017010435.3:c.525+2396_525+2399dup	XM_017010435.3:c.525+2395_525+2399dup	XM_017010435.3:c.525+2394_525+2399dup	XM_017010435.3:c.525+2393_525+2399dup	XM_017010435.3:c.525+2392_525+2399dup	XM_017010435.3:c.525+2391_525+2399dup	XM_017010435.3:c.525+2390_525+2399dup	XM_017010435.3:c.525+2386_525+2399dup
ARMC12 transcript variant X5	XM_047418343.1:c.525+2380=	XM_047418343.1:c.525+2394_525+2399del	XM_047418343.1:c.525+2395_525+2399del	XM_047418343.1:c.525+2396_525+2399del	XM_047418343.1:c.525+2397_525+2399del	XM_047418343.1:c.525+2398_525+2399del	XM_047418343.1:c.525+2399del	XM_047418343.1:c.525+2399dup	XM_047418343.1:c.525+2398_525+2399dup	XM_047418343.1:c.525+2397_525+2399dup	XM_047418343.1:c.525+2396_525+2399dup	XM_047418343.1:c.525+2395_525+2399dup	XM_047418343.1:c.525+2394_525+2399dup	XM_047418343.1:c.525+2393_525+2399dup	XM_047418343.1:c.525+2392_525+2399dup	XM_047418343.1:c.525+2391_525+2399dup	XM_047418343.1:c.525+2390_525+2399dup	XM_047418343.1:c.525+2386_525+2399dup
ARMC12 transcript variant X6	XM_047418344.1:c.525+2380=	XM_047418344.1:c.525+2394_525+2399del	XM_047418344.1:c.525+2395_525+2399del	XM_047418344.1:c.525+2396_525+2399del	XM_047418344.1:c.525+2397_525+2399del	XM_047418344.1:c.525+2398_525+2399del	XM_047418344.1:c.525+2399del	XM_047418344.1:c.525+2399dup	XM_047418344.1:c.525+2398_525+2399dup	XM_047418344.1:c.525+2397_525+2399dup	XM_047418344.1:c.525+2396_525+2399dup	XM_047418344.1:c.525+2395_525+2399dup	XM_047418344.1:c.525+2394_525+2399dup	XM_047418344.1:c.525+2393_525+2399dup	XM_047418344.1:c.525+2392_525+2399dup	XM_047418344.1:c.525+2391_525+2399dup	XM_047418344.1:c.525+2390_525+2399dup	XM_047418344.1:c.525+2386_525+2399dup
ARMC12 transcript variant X7	XM_047418345.1:c.525+2380=	XM_047418345.1:c.525+2394_525+2399del	XM_047418345.1:c.525+2395_525+2399del	XM_047418345.1:c.525+2396_525+2399del	XM_047418345.1:c.525+2397_525+2399del	XM_047418345.1:c.525+2398_525+2399del	XM_047418345.1:c.525+2399del	XM_047418345.1:c.525+2399dup	XM_047418345.1:c.525+2398_525+2399dup	XM_047418345.1:c.525+2397_525+2399dup	XM_047418345.1:c.525+2396_525+2399dup	XM_047418345.1:c.525+2395_525+2399dup	XM_047418345.1:c.525+2394_525+2399dup	XM_047418345.1:c.525+2393_525+2399dup	XM_047418345.1:c.525+2392_525+2399dup	XM_047418345.1:c.525+2391_525+2399dup	XM_047418345.1:c.525+2390_525+2399dup	XM_047418345.1:c.525+2386_525+2399dup
ARMC12 transcript variant X8	XM_047418346.1:c.525+2380=	XM_047418346.1:c.525+2394_525+2399del	XM_047418346.1:c.525+2395_525+2399del	XM_047418346.1:c.525+2396_525+2399del	XM_047418346.1:c.525+2397_525+2399del	XM_047418346.1:c.525+2398_525+2399del	XM_047418346.1:c.525+2399del	XM_047418346.1:c.525+2399dup	XM_047418346.1:c.525+2398_525+2399dup	XM_047418346.1:c.525+2397_525+2399dup	XM_047418346.1:c.525+2396_525+2399dup	XM_047418346.1:c.525+2395_525+2399dup	XM_047418346.1:c.525+2394_525+2399dup	XM_047418346.1:c.525+2393_525+2399dup	XM_047418346.1:c.525+2392_525+2399dup	XM_047418346.1:c.525+2391_525+2399dup	XM_047418346.1:c.525+2390_525+2399dup	XM_047418346.1:c.525+2386_525+2399dup
ARMC12 transcript variant X9	XM_047418347.1:c.444+2380=	XM_047418347.1:c.444+2394_444+2399del	XM_047418347.1:c.444+2395_444+2399del	XM_047418347.1:c.444+2396_444+2399del	XM_047418347.1:c.444+2397_444+2399del	XM_047418347.1:c.444+2398_444+2399del	XM_047418347.1:c.444+2399del	XM_047418347.1:c.444+2399dup	XM_047418347.1:c.444+2398_444+2399dup	XM_047418347.1:c.444+2397_444+2399dup	XM_047418347.1:c.444+2396_444+2399dup	XM_047418347.1:c.444+2395_444+2399dup	XM_047418347.1:c.444+2394_444+2399dup	XM_047418347.1:c.444+2393_444+2399dup	XM_047418347.1:c.444+2392_444+2399dup	XM_047418347.1:c.444+2391_444+2399dup	XM_047418347.1:c.444+2390_444+2399dup	XM_047418347.1:c.444+2386_444+2399dup
ARMC12 transcript variant X1	XM_047418348.1:c.444+2380=	XM_047418348.1:c.444+2394_444+2399del	XM_047418348.1:c.444+2395_444+2399del	XM_047418348.1:c.444+2396_444+2399del	XM_047418348.1:c.444+2397_444+2399del	XM_047418348.1:c.444+2398_444+2399del	XM_047418348.1:c.444+2399del	XM_047418348.1:c.444+2399dup	XM_047418348.1:c.444+2398_444+2399dup	XM_047418348.1:c.444+2397_444+2399dup	XM_047418348.1:c.444+2396_444+2399dup	XM_047418348.1:c.444+2395_444+2399dup	XM_047418348.1:c.444+2394_444+2399dup	XM_047418348.1:c.444+2393_444+2399dup	XM_047418348.1:c.444+2392_444+2399dup	XM_047418348.1:c.444+2391_444+2399dup	XM_047418348.1:c.444+2390_444+2399dup	XM_047418348.1:c.444+2386_444+2399dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

61 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42763027	Mar 13, 2006 (126)
2	BL	ss256063372	May 09, 2011 (137)
3	SSMP	ss663692023	Apr 01, 2015 (144)
4	SSIP	ss947167075	Aug 21, 2014 (142)
5	EVA_UK10K_ALSPAC	ss1705119990	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1705120164	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1710264323	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710264325	Jan 10, 2018 (151)
9	EVA_UK10K_ALSPAC	ss1710264333	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710264335	Jan 10, 2018 (151)
11	SWEGEN	ss2998886285	Nov 08, 2017 (151)
12	PACBIO	ss3790800660	Jul 13, 2019 (153)
13	PACBIO	ss3790800661	Jul 13, 2019 (153)
14	PACBIO	ss3795679283	Jul 13, 2019 (153)
15	PACBIO	ss3795679284	Jul 13, 2019 (153)
16	EVA	ss3829866498	Apr 26, 2020 (154)
17	KOGIC	ss3958801617	Apr 26, 2020 (154)
18	KOGIC	ss3958801618	Apr 26, 2020 (154)
19	KOGIC	ss3958801619	Apr 26, 2020 (154)
20	KOGIC	ss3958801620	Apr 26, 2020 (154)
21	KOGIC	ss3958801621	Apr 26, 2020 (154)
22	KOGIC	ss3958801622	Apr 26, 2020 (154)
23	GNOMAD	ss4139854847	Apr 26, 2021 (155)
24	GNOMAD	ss4139854848	Apr 26, 2021 (155)
25	GNOMAD	ss4139854849	Apr 26, 2021 (155)
26	GNOMAD	ss4139854850	Apr 26, 2021 (155)
27	GNOMAD	ss4139854851	Apr 26, 2021 (155)
28	GNOMAD	ss4139854852	Apr 26, 2021 (155)
29	GNOMAD	ss4139854853	Apr 26, 2021 (155)
30	GNOMAD	ss4139854854	Apr 26, 2021 (155)
31	GNOMAD	ss4139854855	Apr 26, 2021 (155)
32	GNOMAD	ss4139854856	Apr 26, 2021 (155)
33	GNOMAD	ss4139854857	Apr 26, 2021 (155)
34	GNOMAD	ss4139854859	Apr 26, 2021 (155)
35	GNOMAD	ss4139854860	Apr 26, 2021 (155)
36	GNOMAD	ss4139854861	Apr 26, 2021 (155)
37	GNOMAD	ss4139854862	Apr 26, 2021 (155)
38	GNOMAD	ss4139854863	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5177013355	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5177013356	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5177013357	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5177013358	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5177013359	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5177013360	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5268056391	Oct 17, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5268056392	Oct 17, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5268056393	Oct 17, 2022 (156)
48	HUGCELL_USP	ss5465767220	Oct 17, 2022 (156)
49	HUGCELL_USP	ss5465767221	Oct 17, 2022 (156)
50	HUGCELL_USP	ss5465767222	Oct 17, 2022 (156)
51	HUGCELL_USP	ss5465767223	Oct 17, 2022 (156)
52	HUGCELL_USP	ss5465767224	Oct 17, 2022 (156)
53	TOMMO_GENOMICS	ss5714915629	Oct 17, 2022 (156)
54	TOMMO_GENOMICS	ss5714915630	Oct 17, 2022 (156)
55	TOMMO_GENOMICS	ss5714915631	Oct 17, 2022 (156)
56	TOMMO_GENOMICS	ss5714915632	Oct 17, 2022 (156)
57	TOMMO_GENOMICS	ss5714915633	Oct 17, 2022 (156)
58	EVA	ss5842088229	Oct 17, 2022 (156)
59	EVA	ss5842088230	Oct 17, 2022 (156)
60	EVA	ss5842088231	Oct 17, 2022 (156)
61	EVA	ss5855310695	Oct 17, 2022 (156)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17537752 (NC_000006.11:35708674:TTT: 395/3854) Row 17537753 (NC_000006.11:35708675:T: 1447/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17537752 (NC_000006.11:35708674:TTT: 395/3854) Row 17537753 (NC_000006.11:35708675:T: 1447/3854)	-	Oct 12, 2018 (152)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035610 (NC_000006.12:35740897::T 16427/106616) Row 222035611 (NC_000006.12:35740897::TT 2590/106602) Row 222035612 (NC_000006.12:35740897::TTT 1288/106608)...	-	Apr 26, 2021 (155)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 15179618 (NC_000006.12:35740899::T 305/1830) Row 15179619 (NC_000006.12:35740899::TT 32/1830) Row 15179620 (NC_000006.12:35740898:T: 489/1830)...	-	Apr 26, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 15179618 (NC_000006.12:35740899::T 305/1830) Row 15179619 (NC_000006.12:35740899::TT 32/1830) Row 15179620 (NC_000006.12:35740898:T: 489/1830)...	-	Apr 26, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 15179618 (NC_000006.12:35740899::T 305/1830) Row 15179619 (NC_000006.12:35740899::TT 32/1830) Row 15179620 (NC_000006.12:35740898:T: 489/1830)...	-	Apr 26, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 15179618 (NC_000006.12:35740899::T 305/1830) Row 15179619 (NC_000006.12:35740899::TT 32/1830) Row 15179620 (NC_000006.12:35740898:T: 489/1830)...	-	Apr 26, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 15179618 (NC_000006.12:35740899::T 305/1830) Row 15179619 (NC_000006.12:35740899::TT 32/1830) Row 15179620 (NC_000006.12:35740898:T: 489/1830)...	-	Apr 26, 2020 (154)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 15179618 (NC_000006.12:35740899::T 305/1830) Row 15179619 (NC_000006.12:35740899::TT 32/1830) Row 15179620 (NC_000006.12:35740898:T: 489/1830)...	-	Apr 26, 2020 (154)
87	8.3KJPN Submission ignored due to conflicting rows: Row 34982662 (NC_000006.11:35708674::T 2573/16586) Row 34982663 (NC_000006.11:35708674:T: 2895/16586) Row 34982664 (NC_000006.11:35708674::TT 36/16586)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 34982662 (NC_000006.11:35708674::T 2573/16586) Row 34982663 (NC_000006.11:35708674:T: 2895/16586) Row 34982664 (NC_000006.11:35708674::TT 36/16586)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 34982662 (NC_000006.11:35708674::T 2573/16586) Row 34982663 (NC_000006.11:35708674:T: 2895/16586) Row 34982664 (NC_000006.11:35708674::TT 36/16586)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 34982662 (NC_000006.11:35708674::T 2573/16586) Row 34982663 (NC_000006.11:35708674:T: 2895/16586) Row 34982664 (NC_000006.11:35708674::TT 36/16586)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 34982662 (NC_000006.11:35708674::T 2573/16586) Row 34982663 (NC_000006.11:35708674:T: 2895/16586) Row 34982664 (NC_000006.11:35708674::TT 36/16586)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 34982662 (NC_000006.11:35708674::T 2573/16586) Row 34982663 (NC_000006.11:35708674:T: 2895/16586) Row 34982664 (NC_000006.11:35708674::TT 36/16586)...	-	Apr 26, 2021 (155)
93	14KJPN Submission ignored due to conflicting rows: Row 48752733 (NC_000006.12:35740897::T 4487/28006) Row 48752734 (NC_000006.12:35740897:T: 5150/28006) Row 48752735 (NC_000006.12:35740897::TTTTTTT 449/28006)...	-	Oct 17, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 48752733 (NC_000006.12:35740897::T 4487/28006) Row 48752734 (NC_000006.12:35740897:T: 5150/28006) Row 48752735 (NC_000006.12:35740897::TTTTTTT 449/28006)...	-	Oct 17, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 48752733 (NC_000006.12:35740897::T 4487/28006) Row 48752734 (NC_000006.12:35740897:T: 5150/28006) Row 48752735 (NC_000006.12:35740897::TTTTTTT 449/28006)...	-	Oct 17, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 48752733 (NC_000006.12:35740897::T 4487/28006) Row 48752734 (NC_000006.12:35740897:T: 5150/28006) Row 48752735 (NC_000006.12:35740897::TTTTTTT 449/28006)...	-	Oct 17, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 48752733 (NC_000006.12:35740897::T 4487/28006) Row 48752734 (NC_000006.12:35740897:T: 5150/28006) Row 48752735 (NC_000006.12:35740897::TTTTTTT 449/28006)...	-	Oct 17, 2022 (156)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17537751 (NC_000006.11:35708676:T: 1272/3708) Row 17537752 (NC_000006.11:35708674:TTT: 347/3708) Row 17537753 (NC_000006.11:35708675:TT: 1348/3708)	-	Apr 26, 2020 (154)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17537752 (NC_000006.11:35708674:TTT: 347/3708) Row 17537753 (NC_000006.11:35708675:T: 1348/3708)	-	Oct 12, 2018 (152)
100	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17537752 (NC_000006.11:35708674:TTT: 347/3708) Row 17537753 (NC_000006.11:35708675:T: 1348/3708)	-	Oct 12, 2018 (152)
101	ALFA	NC_000006.12 - 35740898	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs796181482	Nov 08, 2017 (151)
rs149552564	May 04, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4139854863	NC_000006.12:35740897:TTTTTT:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4139854862	NC_000006.12:35740897:TTTTT:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4139854861	NC_000006.12:35740897:TTTT:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss1705119990, ss1705120164, ss5842088231	NC_000006.11:35708674:TTT:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4139854860, ss5855310695	NC_000006.12:35740897:TTT:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5842088230	NC_000006.11:35708674:TT:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
ss1710264325, ss1710264335	NC_000006.11:35708675:TT:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3958801620, ss4139854859, ss5465767221	NC_000006.12:35740897:TT:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss256063372	NC_000006.10:35816652:T:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss2998886285, ss3790800660, ss3795679283, ss5177013356, ss5842088229	NC_000006.11:35708674:T:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
	NC_000006.11:35708675:T:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss1710264323, ss1710264333	NC_000006.11:35708676:T:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5268056392, ss5465767220, ss5714915630	NC_000006.12:35740897:T:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3958801619	NC_000006.12:35740898:T:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss42763027	NT_007592.15:35648674:T:	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss663692023, ss3790800661, ss3795679284, ss5177013355	NC_000006.11:35708674::T	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss947167075	NC_000006.11:35708676::T	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854847, ss5268056391, ss5465767222, ss5714915629	NC_000006.12:35740897::T	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3958801617	NC_000006.12:35740899::T	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3829866498, ss5177013357	NC_000006.11:35708674::TT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854848, ss5268056393, ss5465767223, ss5714915632	NC_000006.12:35740897::TT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3958801618	NC_000006.12:35740899::TT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854849, ss5465767224	NC_000006.12:35740897::TTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854850	NC_000006.12:35740897::TTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854851	NC_000006.12:35740897::TTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854852	NC_000006.12:35740897::TTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3958801621	NC_000006.12:35740899::TTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5177013358	NC_000006.11:35708674::TTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854853, ss5714915631	NC_000006.12:35740897::TTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3958801622	NC_000006.12:35740899::TTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5177013359	NC_000006.11:35708674::TTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854854, ss5714915633	NC_000006.12:35740897::TTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3576696505	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5177013360	NC_000006.11:35708674::TTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854855	NC_000006.12:35740897::TTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854856	NC_000006.12:35740897::TTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139854857	NC_000006.12:35740897::TTTTTTTTTTT… NC_000006.12:35740897::TTTTTTTTTTTTTT	NC_000006.12:35740897:TTTTTTTTTTTT… NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs11365534

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11365534