Name: rs201090239
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.

rs201090239

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:34446941-34446957 (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(A)₈ / del(A)₇ / del(A)₅ / del(…
del(A)₈ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆ / dup(A)₈ / dup(A)₁₁ / dup(A)₁₄ / dup(A)₁₅ / dup(A)₁₇ / ins(A)₁₈ / ins(A)₂₀ / ins(A)₂₄G(A)₅(GAA)₂AG(A)₁₈ / ins(AAAAAAAAGAAAA)₂AAAAAAAAAAAAAA / ins(A)₅C(AAAAGA)₂AAAAAG(A)₁₈ / ins(A)₄G(A)₁₈ / ins(A)₄G(A)₁₄(GAAA)₂AAAAAAAAAAAAAAA / ins(AAAAGA)₂AAAAAG(A)₁₈ / ins(AAAAGA)₂AG(A)₅(GAAA)₂AAAAAAAAAAAAAAA
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.11047 (1190/10772, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00457 : Intron Variant
LINC02343 : 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	10772	AAAAAAAAAAAAAAAAA=0.88498	AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.11047, AAAAAAAAAAAAAAAAAA=0.00130, AAAAAAAAAAAAAAAA=0.00232, AAAAAAAAAAAAAAAAAAAAA=0.00074, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00019, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000	0.818063	0.038973	0.142964	32
European	Sub	9388	AAAAAAAAAAAAAAAAA=0.8684	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.1263, AAAAAAAAAAAAAAAAAA=0.0015, AAAAAAAAAAAAAAAA=0.0027, AAAAAAAAAAAAAAAAAAAAA=0.0009, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0002, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	0.791819	0.044779	0.163402	32
African	Sub	816	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	20	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	796	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	16	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	60	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	214	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	52	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	226	AAAAAAAAAAAAAAAAA=0.982	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.018, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	0.964602	0.0	0.035398	0

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	10772	(A)₁₇=0.88498	del(A)₈=0.00000, del(A)₇=0.00000, del(A)₅=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.11047, delA=0.00232, dupA=0.00130, dupAA=0.00000, dupAAA=0.00000, dup(A)₄=0.00074, ins(A)₁₈=0.00019
Allele Frequency Aggregator	European	Sub	9388	(A)₁₇=0.8684	del(A)₈=0.0000, del(A)₇=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.1263, delA=0.0027, dupA=0.0015, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0009, ins(A)₁₈=0.0002
Allele Frequency Aggregator	African	Sub	816	(A)₁₇=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, ins(A)₁₈=0.000
Allele Frequency Aggregator	Other	Sub	226	(A)₁₇=0.982	del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.018, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, ins(A)₁₈=0.000
Allele Frequency Aggregator	Latin American 2	Sub	214	(A)₁₇=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, ins(A)₁₈=0.000
Allele Frequency Aggregator	Latin American 1	Sub	60	(A)₁₇=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, ins(A)₁₈=0.00
Allele Frequency Aggregator	South Asian	Sub	52	(A)₁₇=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, ins(A)₁₈=0.00
Allele Frequency Aggregator	Asian	Sub	16	(A)₁₇=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, ins(A)₁₈=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 13	NC_000013.11:g.34446950_34446957del
GRCh38.p14 chr 13	NC_000013.11:g.34446951_34446957del
GRCh38.p14 chr 13	NC_000013.11:g.34446953_34446957del
GRCh38.p14 chr 13	NC_000013.11:g.34446954_34446957del
GRCh38.p14 chr 13	NC_000013.11:g.34446955_34446957del
GRCh38.p14 chr 13	NC_000013.11:g.34446956_34446957del
GRCh38.p14 chr 13	NC_000013.11:g.34446957del
GRCh38.p14 chr 13	NC_000013.11:g.34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446956_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446955_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446954_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446952_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446950_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446947_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446944_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446943_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957dup
GRCh38.p14 chr 13	NC_000013.11:g.34446957_34446958insAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.34446957_34446958insAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957A[41]GAAAAAGAAGAAAGAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957A[25]GAAAAAAAAAAAA[2]A[6]
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957A[22]CAAAAGAAAAAGAAAAAAGAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957A[21]GAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957A[21]GAAAAAAAAAAAAAAGAAAGAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957A[21]GAAAAA[2]AGAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957A[21]GAAAAAGAA[2]AGAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 13	NC_000013.10:g.35021087_35021094del
GRCh37.p13 chr 13	NC_000013.10:g.35021088_35021094del
GRCh37.p13 chr 13	NC_000013.10:g.35021090_35021094del
GRCh37.p13 chr 13	NC_000013.10:g.35021091_35021094del
GRCh37.p13 chr 13	NC_000013.10:g.35021092_35021094del
GRCh37.p13 chr 13	NC_000013.10:g.35021093_35021094del
GRCh37.p13 chr 13	NC_000013.10:g.35021094del
GRCh37.p13 chr 13	NC_000013.10:g.35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021093_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021092_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021091_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021089_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021087_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021084_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021081_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021080_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094dup
GRCh37.p13 chr 13	NC_000013.10:g.35021094_35021095insAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.35021094_35021095insAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094A[41]GAAAAAGAAGAAAGAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094A[25]GAAAAAAAAAAAA[2]A[6]
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094A[22]CAAAAGAAAAAGAAAAAAGAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094A[21]GAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094A[21]GAAAAAAAAAAAAAAGAAAGAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094A[21]GAAAAA[2]AGAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094A[21]GAAAAAGAA[2]AGAAAAAAAAAAAAAAAAAA[1]

Gene: LINC00457, long intergenic non-protein coding RNA 457 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00457 transcript	NR_047036.1:n.	N/A	Intron Variant

Gene: LINC02343, long intergenic non-protein coding RNA 2343 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02343 transcript	NR_146542.1:n.	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	(A)₁₇=	del(A)₈	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆	dup(A)₈	dup(A)₁₁	dup(A)₁₄	dup(A)₁₅	dup(A)₁₇	ins(A)₁₈	ins(A)₂₀	ins(A)₂₄G(A)₅(GAA)₂AG(A)₁₈	ins(AAAAAAAAGAAAA)₂AAAAAAAAAAAAAA	ins(A)₅C(AAAAGA)₂AAAAAG(A)₁₈	ins(A)₄G(A)₁₈	ins(A)₄G(A)₁₄(GAAA)₂AAAAAAAAAAAAAAA	ins(AAAAGA)₂AAAAAG(A)₁₈	ins(AAAAGA)₂AG(A)₅(GAAA)₂AAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.34446941_34446957=	NC_000013.11:g.34446950_34446957del	NC_000013.11:g.34446951_34446957del	NC_000013.11:g.34446953_34446957del	NC_000013.11:g.34446954_34446957del	NC_000013.11:g.34446955_34446957del	NC_000013.11:g.34446956_34446957del	NC_000013.11:g.34446957del	NC_000013.11:g.34446957dup	NC_000013.11:g.34446956_34446957dup	NC_000013.11:g.34446955_34446957dup	NC_000013.11:g.34446954_34446957dup	NC_000013.11:g.34446952_34446957dup	NC_000013.11:g.34446950_34446957dup	NC_000013.11:g.34446947_34446957dup	NC_000013.11:g.34446944_34446957dup	NC_000013.11:g.34446943_34446957dup	NC_000013.11:g.34446941_34446957dup	NC_000013.11:g.34446957_34446958insAAAAAAAAAAAAAAAAAA	NC_000013.11:g.34446957_34446958insAAAAAAAAAAAAAAAAAAAA	NC_000013.11:g.34446941_34446957A[41]GAAAAAGAAGAAAGAAAAAAAAAAAAAAAAAA[1]	NC_000013.11:g.34446941_34446957A[25]GAAAAAAAAAAAA[2]A[6]	NC_000013.11:g.34446941_34446957A[22]CAAAAGAAAAAGAAAAAAGAAAAAAAAAAAAAAAAAA[1]	NC_000013.11:g.34446941_34446957A[21]GAAAAAAAAAAAAAAAAAA[1]	NC_000013.11:g.34446941_34446957A[21]GAAAAAAAAAAAAAAGAAAGAAAAAAAAAAAAAAAAAA[1]	NC_000013.11:g.34446941_34446957A[21]GAAAAA[2]AGAAAAAAAAAAAAAAAAAA[1]	NC_000013.11:g.34446941_34446957A[21]GAAAAAGAA[2]AGAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 13	NC_000013.10:g.35021078_35021094=	NC_000013.10:g.35021087_35021094del	NC_000013.10:g.35021088_35021094del	NC_000013.10:g.35021090_35021094del	NC_000013.10:g.35021091_35021094del	NC_000013.10:g.35021092_35021094del	NC_000013.10:g.35021093_35021094del	NC_000013.10:g.35021094del	NC_000013.10:g.35021094dup	NC_000013.10:g.35021093_35021094dup	NC_000013.10:g.35021092_35021094dup	NC_000013.10:g.35021091_35021094dup	NC_000013.10:g.35021089_35021094dup	NC_000013.10:g.35021087_35021094dup	NC_000013.10:g.35021084_35021094dup	NC_000013.10:g.35021081_35021094dup	NC_000013.10:g.35021080_35021094dup	NC_000013.10:g.35021078_35021094dup	NC_000013.10:g.35021094_35021095insAAAAAAAAAAAAAAAAAA	NC_000013.10:g.35021094_35021095insAAAAAAAAAAAAAAAAAAAA	NC_000013.10:g.35021078_35021094A[41]GAAAAAGAAGAAAGAAAAAAAAAAAAAAAAAA[1]	NC_000013.10:g.35021078_35021094A[25]GAAAAAAAAAAAA[2]A[6]	NC_000013.10:g.35021078_35021094A[22]CAAAAGAAAAAGAAAAAAGAAAAAAAAAAAAAAAAAA[1]	NC_000013.10:g.35021078_35021094A[21]GAAAAAAAAAAAAAAAAAA[1]	NC_000013.10:g.35021078_35021094A[21]GAAAAAAAAAAAAAAGAAAGAAAAAAAAAAAAAAAAAA[1]	NC_000013.10:g.35021078_35021094A[21]GAAAAA[2]AGAAAAAAAAAAAAAAAAAA[1]	NC_000013.10:g.35021078_35021094A[21]GAAAAAGAA[2]AGAAAAAAAAAAAAAAAAAA[1]

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#.

60 SubSNP, 37 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss289170613	May 04, 2012 (137)
2	SSMP	ss664172450	Apr 01, 2015 (144)
3	BILGI_BIOE	ss666594838	Apr 25, 2013 (138)
4	SYSTEMSBIOZJU	ss2628277998	Nov 08, 2017 (151)
5	SWEGEN	ss3010842161	Nov 08, 2017 (151)
6	MCHAISSO	ss3065514540	Nov 08, 2017 (151)
7	EVA_DECODE	ss3695074827	Jul 13, 2019 (153)
8	EVA_DECODE	ss3695074828	Jul 13, 2019 (153)
9	EVA_DECODE	ss3695074829	Jul 13, 2019 (153)
10	EVA_DECODE	ss3695074830	Jul 13, 2019 (153)
11	ACPOP	ss3739650000	Jul 13, 2019 (153)
12	ACPOP	ss3739650001	Jul 13, 2019 (153)
13	PACBIO	ss3787426603	Jul 13, 2019 (153)
14	EVA	ss3833489533	Apr 27, 2020 (154)
15	EVA	ss3840322968	Apr 27, 2020 (154)
16	EVA	ss3845808002	Apr 27, 2020 (154)
17	GNOMAD	ss4263968811	Apr 26, 2021 (155)
18	GNOMAD	ss4263968812	Apr 26, 2021 (155)
19	GNOMAD	ss4263968813	Apr 26, 2021 (155)
20	GNOMAD	ss4263968814	Apr 26, 2021 (155)
21	GNOMAD	ss4263968815	Apr 26, 2021 (155)
22	GNOMAD	ss4263968816	Apr 26, 2021 (155)
23	GNOMAD	ss4263968817	Apr 26, 2021 (155)
24	GNOMAD	ss4263968818	Apr 26, 2021 (155)
25	GNOMAD	ss4263968819	Apr 26, 2021 (155)
26	GNOMAD	ss4263968820	Apr 26, 2021 (155)
27	GNOMAD	ss4263968821	Apr 26, 2021 (155)
28	GNOMAD	ss4263968822	Apr 26, 2021 (155)
29	GNOMAD	ss4263968823	Apr 26, 2021 (155)
30	GNOMAD	ss4263968824	Apr 26, 2021 (155)
31	GNOMAD	ss4263968825	Apr 26, 2021 (155)
32	GNOMAD	ss4263968826	Apr 26, 2021 (155)
33	GNOMAD	ss4263968827	Apr 26, 2021 (155)
34	GNOMAD	ss4263968828	Apr 26, 2021 (155)
35	GNOMAD	ss4263968829	Apr 26, 2021 (155)
36	GNOMAD	ss4263968830	Apr 26, 2021 (155)
37	GNOMAD	ss4263968831	Apr 26, 2021 (155)
38	GNOMAD	ss4263968832	Apr 26, 2021 (155)
39	GNOMAD	ss4263968833	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5209503616	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5209503617	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5209503618	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5209503619	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5209503620	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5293354344	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5293354345	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5293354346	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5293354347	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5487756453	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5487756454	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5487756455	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5487756456	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5761239046	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5761239047	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5761239048	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5761239049	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5761239050	Oct 16, 2022 (156)
58	EVA	ss5839325053	Oct 16, 2022 (156)
59	EVA	ss5839325054	Oct 16, 2022 (156)
60	EVA	ss5839325055	Oct 16, 2022 (156)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427585885 (NC_000013.11:34446940::A 806/106986) Row 427585886 (NC_000013.11:34446940::AA 12/107014) Row 427585887 (NC_000013.11:34446940::AAA 4/107014)...	-	Apr 26, 2021 (155)
85	Northern Sweden Submission ignored due to conflicting rows: Row 12934865 (NC_000013.10:35021077:AA: 143/560) Row 12934866 (NC_000013.10:35021077::AAA 1/560)	-	Jul 13, 2019 (153)
86	Northern Sweden Submission ignored due to conflicting rows: Row 12934865 (NC_000013.10:35021077:AA: 143/560) Row 12934866 (NC_000013.10:35021077::AAA 1/560)	-	Jul 13, 2019 (153)
87	8.3KJPN Submission ignored due to conflicting rows: Row 67472923 (NC_000013.10:35021077:AA: 13068/16750) Row 67472924 (NC_000013.10:35021077:AAA: 707/16750) Row 67472925 (NC_000013.10:35021077:A: 363/16750)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 67472923 (NC_000013.10:35021077:AA: 13068/16750) Row 67472924 (NC_000013.10:35021077:AAA: 707/16750) Row 67472925 (NC_000013.10:35021077:A: 363/16750)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 67472923 (NC_000013.10:35021077:AA: 13068/16750) Row 67472924 (NC_000013.10:35021077:AAA: 707/16750) Row 67472925 (NC_000013.10:35021077:A: 363/16750)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 67472923 (NC_000013.10:35021077:AA: 13068/16750) Row 67472924 (NC_000013.10:35021077:AAA: 707/16750) Row 67472925 (NC_000013.10:35021077:A: 363/16750)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 67472923 (NC_000013.10:35021077:AA: 13068/16750) Row 67472924 (NC_000013.10:35021077:AAA: 707/16750) Row 67472925 (NC_000013.10:35021077:A: 363/16750)...	-	Apr 26, 2021 (155)
92	14KJPN Submission ignored due to conflicting rows: Row 95076150 (NC_000013.11:34446940:AA: 22114/28238) Row 95076151 (NC_000013.11:34446940:AAA: 1208/28238) Row 95076152 (NC_000013.11:34446940:A: 624/28238)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 95076150 (NC_000013.11:34446940:AA: 22114/28238) Row 95076151 (NC_000013.11:34446940:AAA: 1208/28238) Row 95076152 (NC_000013.11:34446940:A: 624/28238)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 95076150 (NC_000013.11:34446940:AA: 22114/28238) Row 95076151 (NC_000013.11:34446940:AAA: 1208/28238) Row 95076152 (NC_000013.11:34446940:A: 624/28238)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 95076150 (NC_000013.11:34446940:AA: 22114/28238) Row 95076151 (NC_000013.11:34446940:AAA: 1208/28238) Row 95076152 (NC_000013.11:34446940:A: 624/28238)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 95076150 (NC_000013.11:34446940:AA: 22114/28238) Row 95076151 (NC_000013.11:34446940:AAA: 1208/28238) Row 95076152 (NC_000013.11:34446940:A: 624/28238)...	-	Oct 16, 2022 (156)
97	ALFA	NC_000013.11 - 34446941	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss5209503620	NC_000013.10:35021077:AAAAAAA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4263968833, ss5761239050	NC_000013.11:34446940:AAAAAAA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4263968832	NC_000013.11:34446940:AAAAA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4263968831	NC_000013.11:34446940:AAAA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3010842161, ss5209503617, ss5839325054	NC_000013.10:35021077:AAA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3695074830, ss4263968830, ss5293354346, ss5487756453, ss5761239047	NC_000013.11:34446940:AAA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss289170613	NC_000013.9:33919077:AA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss664172450, ss666594838, ss2628277998, ss3739650000, ss3833489533, ss3840322968, ss5209503616, ss5839325053	NC_000013.10:35021077:AA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3065514540, ss3845808002, ss4263968829, ss5293354344, ss5487756454, ss5761239046	NC_000013.11:34446940:AA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3695074829	NC_000013.11:34446941:AA:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3787426603, ss5209503618	NC_000013.10:35021077:A:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4263968828, ss5293354345, ss5487756455, ss5761239048	NC_000013.11:34446940:A:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3695074828	NC_000013.11:34446942:A:	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5209503619	NC_000013.10:35021077::A	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4263968811, ss5293354347, ss5487756456, ss5761239049	NC_000013.11:34446940::A	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3695074827	NC_000013.11:34446943::A	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4263968812	NC_000013.11:34446940::AA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3739650001	NC_000013.10:35021077::AAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4263968813	NC_000013.11:34446940::AAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5839325055	NC_000013.10:35021077::AAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA
ss4263968814	NC_000013.11:34446940::AAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4263968815	NC_000013.11:34446940::AAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4263968816	NC_000013.11:34446940::AAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4263968817	NC_000013.11:34446940::AAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4263968818	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4263968819	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4263968820	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10797758466	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4263968821	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAAAAA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAGAAGAAAGA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAGAAGAAAGAAAAAAAAAAAAAAAAAA	(self)
ss4263968822	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAGA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAA	(self)
ss4263968823	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAAAAAAACAAAAGAAAAAGAAAAAAGA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACAAAAGAAAAAGAAAAAAGAAAAAAAAAAAAAAAAAA	(self)
ss4263968824	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAAAAAAGA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAA	(self)
ss4263968825	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAGAAAGA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAGAAAGAAAAAAAAAAAAAAAAAA	(self)
ss4263968826	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAAAAAAGAAAAAGAAAAAAGA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAGAAAAAGAAAAAAGAAAAAAAAAAAAAAAAAA	(self)
ss4263968827	NC_000013.11:34446940::AAAAAAAAAAA… NC_000013.11:34446940::AAAAAAAAAAAAAAAAAAAAAGAAAAAGAAGAAAAAGAAAGA	NC_000013.11:34446940:AAAAAAAAAAAA… NC_000013.11:34446940:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAGAAAAAGAAGAAAAAGAAAGAAAAAAAAAAAAAAAAAA	(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 rs201090239

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

rs201090239