Name: rs36182126
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.

rs36182126

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:49561027-49561053 (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(CT)₅ / del(CT)₄ / del(CT)₃ / d…
del(CT)₅ / del(CT)₄ / del(CT)₃ / delCTCT / delCT / dupCT / dupCTCT / dup(CT)₃ / dup(CT)₄ / dup(CT)₅ / dup(CT)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupCT=0.3569 (2499/7002, ALFA)
dupCT=0.4718 (2363/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: C6orf141 : 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	7002	TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.6361	TCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCT=0.0009, TCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.3569, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0034, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0027, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	0.484796	0.200116	0.315088	32
European	Sub	6054	TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.5796	TCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCT=0.0010, TCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.4123, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0040, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0031, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	0.403827	0.231957	0.364216	32
African	Sub	744	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
African American	Sub	718	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	22	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.0	TCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	14	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	40	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	18	TCTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Other	Sub	110	TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.973	TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.027, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	0.945455	0.0	0.054545	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	7002	(TC)₁₃T=0.6361	del(CT)₅=0.0000, del(CT)₄=0.0000, del(CT)₃=0.0009, delCTCT=0.0000, delCT=0.0000, dupCT=0.3569, dupCTCT=0.0027, dup(CT)₃=0.0034, dup(CT)₄=0.0000, dup(CT)₅=0.0000, dup(CT)₆=0.0000
Allele Frequency Aggregator	European	Sub	6054	(TC)₁₃T=0.5796	del(CT)₅=0.0000, del(CT)₄=0.0000, del(CT)₃=0.0010, delCTCT=0.0000, delCT=0.0000, dupCT=0.4123, dupCTCT=0.0031, dup(CT)₃=0.0040, dup(CT)₄=0.0000, dup(CT)₅=0.0000, dup(CT)₆=0.0000
Allele Frequency Aggregator	African	Sub	744	(TC)₁₃T=1.000	del(CT)₅=0.000, del(CT)₄=0.000, del(CT)₃=0.000, delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000, dup(CT)₅=0.000, dup(CT)₆=0.000
Allele Frequency Aggregator	Other	Sub	110	(TC)₁₃T=0.973	del(CT)₅=0.000, del(CT)₄=0.000, del(CT)₃=0.000, delCTCT=0.000, delCT=0.000, dupCT=0.027, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000, dup(CT)₅=0.000, dup(CT)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	40	(TC)₁₃T=1.00	del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
Allele Frequency Aggregator	Asian	Sub	22	(TC)₁₃T=1.00	del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(TC)₁₃T=1.00	del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(TC)₁₃T=1.00	del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₅=0.00, dup(CT)₆=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupCT=0.4718
1000Genomes	African	Sub	1322	- No frequency provided	dupCT=0.3782
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupCT=0.5476
1000Genomes	Europe	Sub	1006	- No frequency provided	dupCT=0.4841
1000Genomes	South Asian	Sub	978	- No frequency provided	dupCT=0.421
1000Genomes	American	Sub	694	- No frequency provided	dupCT=0.594

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.49561028CT[8]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[9]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[10]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[11]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[12]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[14]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[15]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[16]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[17]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[18]
GRCh38.p14 chr 6	NC_000006.12:g.49561028CT[19]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[8]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[9]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[10]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[11]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[12]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[14]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[15]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[16]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[17]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[18]
GRCh37.p13 chr 6	NC_000006.11:g.49528741CT[19]

Gene: C6orf141, chromosome 6 open reading frame 141 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
C6orf141 transcript variant 1	NM_001145652.2:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant 3	NR_146854.3:n.	N/A	Intron Variant
C6orf141 transcript variant 5	NR_146856.3:n.	N/A	Intron Variant
C6orf141 transcript variant 6	NR_146857.3:n.	N/A	Intron Variant
C6orf141 transcript variant 8	NR_146859.3:n.	N/A	Intron Variant
C6orf141 transcript variant 9	NR_146860.3:n.	N/A	Intron Variant
C6orf141 transcript variant 11	NR_146862.3:n.	N/A	Intron Variant
C6orf141 transcript variant 13	NR_146864.3:n.	N/A	Intron Variant
C6orf141 transcript	NR_170577.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170578.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170579.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170580.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170581.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170582.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170583.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170584.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170585.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170586.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170587.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170588.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170589.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170590.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170591.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170592.1:n.	N/A	Intron Variant
C6orf141 transcript	NR_170593.1:n.	N/A	Intron Variant
C6orf141 transcript variant 2	NR_146853.2:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant 4	NR_146855.2:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant 7	NR_146858.2:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant 10	NR_146861.2:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant 12	NR_146863.2:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170563.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170564.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170565.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170566.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170567.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170568.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170569.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170570.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170571.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170572.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170573.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170574.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170575.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript	NR_170576.1:n.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X1	XM_005248850.4:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X7	XM_005248853.3:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X2	XM_006714997.3:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X3	XM_047418225.1:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X4	XM_047418226.1:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X9	XM_047418227.1:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X5	XM_047418228.1:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X6	XM_047418229.1:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X8	XM_047418230.1:c.	N/A	Genic Downstream Transcript Variant
C6orf141 transcript variant X10	XM_047418231.1:c.	N/A	Genic Downstream Transcript 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	(TC)₁₃T=	del(CT)₅	del(CT)₄	del(CT)₃	delCTCT	delCT	dupCT	dupCTCT	dup(CT)₃	dup(CT)₄	dup(CT)₅	dup(CT)₆
GRCh38.p14 chr 6	NC_000006.12:g.49561027_49561053=	NC_000006.12:g.49561028CT[8]	NC_000006.12:g.49561028CT[9]	NC_000006.12:g.49561028CT[10]	NC_000006.12:g.49561028CT[11]	NC_000006.12:g.49561028CT[12]	NC_000006.12:g.49561028CT[14]	NC_000006.12:g.49561028CT[15]	NC_000006.12:g.49561028CT[16]	NC_000006.12:g.49561028CT[17]	NC_000006.12:g.49561028CT[18]	NC_000006.12:g.49561028CT[19]
GRCh37.p13 chr 6	NC_000006.11:g.49528740_49528766=	NC_000006.11:g.49528741CT[8]	NC_000006.11:g.49528741CT[9]	NC_000006.11:g.49528741CT[10]	NC_000006.11:g.49528741CT[11]	NC_000006.11:g.49528741CT[12]	NC_000006.11:g.49528741CT[14]	NC_000006.11:g.49528741CT[15]	NC_000006.11:g.49528741CT[16]	NC_000006.11:g.49528741CT[17]	NC_000006.11:g.49528741CT[18]	NC_000006.11:g.49528741CT[19]

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#.

78 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42855415	Mar 16, 2006 (126)
2	HGSV	ss82950155	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss95428164	Feb 05, 2009 (130)
4	GMI	ss288722578	May 04, 2012 (137)
5	1000GENOMES	ss326802090	May 09, 2011 (135)
6	1000GENOMES	ss326849881	May 09, 2011 (135)
7	1000GENOMES	ss327097661	May 09, 2011 (135)
8	LUNTER	ss551614077	Apr 25, 2013 (138)
9	LUNTER	ss551797894	Apr 25, 2013 (138)
10	LUNTER	ss553247545	Apr 25, 2013 (138)
11	SSMP	ss663700305	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666353855	Apr 25, 2013 (138)
13	1000GENOMES	ss1375493257	Aug 21, 2014 (142)
14	DDI	ss1536503370	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1705158652	Jan 10, 2018 (151)
16	EVA_UK10K_TWINSUK	ss1705158709	Jan 10, 2018 (151)
17	EVA_UK10K_TWINSUK	ss1710269560	Oct 12, 2018 (152)
18	EVA_UK10K_ALSPAC	ss1710269616	Oct 12, 2018 (152)
19	SWEGEN	ss2999045232	Nov 08, 2017 (151)
20	MCHAISSO	ss3064204611	Jan 10, 2018 (151)
21	MCHAISSO	ss3065083448	Jan 10, 2018 (151)
22	MCHAISSO	ss3066080656	Jan 10, 2018 (151)
23	URBANLAB	ss3648348694	Oct 12, 2018 (152)
24	EVA_DECODE	ss3717188640	Jul 13, 2019 (153)
25	EVA_DECODE	ss3717188641	Jul 13, 2019 (153)
26	EVA_DECODE	ss3717188642	Jul 13, 2019 (153)
27	EVA_DECODE	ss3717188643	Jul 13, 2019 (153)
28	EVA_DECODE	ss3717188644	Jul 13, 2019 (153)
29	ACPOP	ss3733495069	Jul 13, 2019 (153)
30	ACPOP	ss3733495070	Jul 13, 2019 (153)
31	ACPOP	ss3733495071	Jul 13, 2019 (153)
32	PACBIO	ss3785471423	Jul 13, 2019 (153)
33	PACBIO	ss3790822846	Jul 13, 2019 (153)
34	PACBIO	ss3795701516	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3808154496	Jul 13, 2019 (153)
36	EVA	ss3829917681	Apr 26, 2020 (154)
37	EVA	ss3838436694	Apr 26, 2020 (154)
38	EVA	ss3843881562	Apr 26, 2020 (154)
39	KOGIC	ss3959012613	Apr 26, 2020 (154)
40	KOGIC	ss3959012614	Apr 26, 2020 (154)
41	KOGIC	ss3959012615	Apr 26, 2020 (154)
42	KOGIC	ss3959012616	Apr 26, 2020 (154)
43	KOGIC	ss3959012617	Apr 26, 2020 (154)
44	GNOMAD	ss4141552871	Apr 26, 2021 (155)
45	GNOMAD	ss4141552872	Apr 26, 2021 (155)
46	GNOMAD	ss4141552873	Apr 26, 2021 (155)
47	GNOMAD	ss4141552874	Apr 26, 2021 (155)
48	GNOMAD	ss4141552875	Apr 26, 2021 (155)
49	GNOMAD	ss4141552876	Apr 26, 2021 (155)
50	GNOMAD	ss4141552877	Apr 26, 2021 (155)
51	GNOMAD	ss4141552878	Apr 26, 2021 (155)
52	GNOMAD	ss4141552879	Apr 26, 2021 (155)
53	GNOMAD	ss4141552880	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5177455524	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5177455525	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5177455526	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5177455527	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5177455528	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5177455529	Apr 26, 2021 (155)
60	1000G_HIGH_COVERAGE	ss5268408669	Oct 13, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5268408670	Oct 13, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5268408671	Oct 13, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5268408672	Oct 13, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5268408673	Oct 13, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5268408674	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5466085413	Oct 13, 2022 (156)
67	HUGCELL_USP	ss5466085414	Oct 13, 2022 (156)
68	HUGCELL_USP	ss5466085415	Oct 13, 2022 (156)
69	HUGCELL_USP	ss5466085416	Oct 13, 2022 (156)
70	TOMMO_GENOMICS	ss5715487653	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5715487654	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5715487655	Oct 13, 2022 (156)
73	TOMMO_GENOMICS	ss5715487656	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5715487657	Oct 13, 2022 (156)
75	TOMMO_GENOMICS	ss5715487658	Oct 13, 2022 (156)
76	EVA	ss5842227480	Oct 13, 2022 (156)
77	EVA	ss5842227481	Oct 13, 2022 (156)
78	EVA	ss5855353523	Oct 13, 2022 (156)
79	1000Genomes	NC_000006.11 - 49528740	Oct 12, 2018 (152)
80	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17776489 (NC_000006.11:49528739::TC 1761/3854) Row 17776490 (NC_000006.11:49528739:TC: 246/3854)	-	Oct 12, 2018 (152)
81	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17776489 (NC_000006.11:49528739::TC 1761/3854) Row 17776490 (NC_000006.11:49528739:TC: 246/3854)	-	Oct 12, 2018 (152)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 224886011 (NC_000006.12:49561026::TC 67405/133494) Row 224886012 (NC_000006.12:49561026::TCTC 845/133708) Row 224886013 (NC_000006.12:49561026::TCTCTC 1018/133728)...	-	Apr 26, 2021 (155)
92	Korean Genome Project Submission ignored due to conflicting rows: Row 15390614 (NC_000006.12:49561032::TC 1003/1832) Row 15390615 (NC_000006.12:49561030:TC: 40/1832) Row 15390616 (NC_000006.12:49561032::TCTC 12/1832)...	-	Apr 26, 2020 (154)
93	Korean Genome Project Submission ignored due to conflicting rows: Row 15390614 (NC_000006.12:49561032::TC 1003/1832) Row 15390615 (NC_000006.12:49561030:TC: 40/1832) Row 15390616 (NC_000006.12:49561032::TCTC 12/1832)...	-	Apr 26, 2020 (154)
94	Korean Genome Project Submission ignored due to conflicting rows: Row 15390614 (NC_000006.12:49561032::TC 1003/1832) Row 15390615 (NC_000006.12:49561030:TC: 40/1832) Row 15390616 (NC_000006.12:49561032::TCTC 12/1832)...	-	Apr 26, 2020 (154)
95	Korean Genome Project Submission ignored due to conflicting rows: Row 15390614 (NC_000006.12:49561032::TC 1003/1832) Row 15390615 (NC_000006.12:49561030:TC: 40/1832) Row 15390616 (NC_000006.12:49561032::TCTC 12/1832)...	-	Apr 26, 2020 (154)
96	Korean Genome Project Submission ignored due to conflicting rows: Row 15390614 (NC_000006.12:49561032::TC 1003/1832) Row 15390615 (NC_000006.12:49561030:TC: 40/1832) Row 15390616 (NC_000006.12:49561032::TCTC 12/1832)...	-	Apr 26, 2020 (154)
97	Northern Sweden Submission ignored due to conflicting rows: Row 6779934 (NC_000006.11:49528739::TC 276/600) Row 6779935 (NC_000006.11:49528739::TCTCTC 6/600) Row 6779936 (NC_000006.11:49528739::TCTC 3/600)	-	Jul 13, 2019 (153)
98	Northern Sweden Submission ignored due to conflicting rows: Row 6779934 (NC_000006.11:49528739::TC 276/600) Row 6779935 (NC_000006.11:49528739::TCTCTC 6/600) Row 6779936 (NC_000006.11:49528739::TCTC 3/600)	-	Jul 13, 2019 (153)
99	Northern Sweden Submission ignored due to conflicting rows: Row 6779934 (NC_000006.11:49528739::TC 276/600) Row 6779935 (NC_000006.11:49528739::TCTCTC 6/600) Row 6779936 (NC_000006.11:49528739::TCTC 3/600)	-	Jul 13, 2019 (153)
100	8.3KJPN Submission ignored due to conflicting rows: Row 35424831 (NC_000006.11:49528739::TC 10601/16760) Row 35424832 (NC_000006.11:49528739:TC: 63/16760) Row 35424833 (NC_000006.11:49528739::TCTC 46/16760)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 35424831 (NC_000006.11:49528739::TC 10601/16760) Row 35424832 (NC_000006.11:49528739:TC: 63/16760) Row 35424833 (NC_000006.11:49528739::TCTC 46/16760)...	-	Apr 26, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 35424831 (NC_000006.11:49528739::TC 10601/16760) Row 35424832 (NC_000006.11:49528739:TC: 63/16760) Row 35424833 (NC_000006.11:49528739::TCTC 46/16760)...	-	Apr 26, 2021 (155)
103	8.3KJPN Submission ignored due to conflicting rows: Row 35424831 (NC_000006.11:49528739::TC 10601/16760) Row 35424832 (NC_000006.11:49528739:TC: 63/16760) Row 35424833 (NC_000006.11:49528739::TCTC 46/16760)...	-	Apr 26, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 35424831 (NC_000006.11:49528739::TC 10601/16760) Row 35424832 (NC_000006.11:49528739:TC: 63/16760) Row 35424833 (NC_000006.11:49528739::TCTC 46/16760)...	-	Apr 26, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 35424831 (NC_000006.11:49528739::TC 10601/16760) Row 35424832 (NC_000006.11:49528739:TC: 63/16760) Row 35424833 (NC_000006.11:49528739::TCTC 46/16760)...	-	Apr 26, 2021 (155)
106	14KJPN Submission ignored due to conflicting rows: Row 49324757 (NC_000006.12:49561026::TC 17813/28258) Row 49324758 (NC_000006.12:49561026::TCTC 73/28258) Row 49324759 (NC_000006.12:49561026:TC: 94/28258)...	-	Oct 13, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 49324757 (NC_000006.12:49561026::TC 17813/28258) Row 49324758 (NC_000006.12:49561026::TCTC 73/28258) Row 49324759 (NC_000006.12:49561026:TC: 94/28258)...	-	Oct 13, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 49324757 (NC_000006.12:49561026::TC 17813/28258) Row 49324758 (NC_000006.12:49561026::TCTC 73/28258) Row 49324759 (NC_000006.12:49561026:TC: 94/28258)...	-	Oct 13, 2022 (156)
109	14KJPN Submission ignored due to conflicting rows: Row 49324757 (NC_000006.12:49561026::TC 17813/28258) Row 49324758 (NC_000006.12:49561026::TCTC 73/28258) Row 49324759 (NC_000006.12:49561026:TC: 94/28258)...	-	Oct 13, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 49324757 (NC_000006.12:49561026::TC 17813/28258) Row 49324758 (NC_000006.12:49561026::TCTC 73/28258) Row 49324759 (NC_000006.12:49561026:TC: 94/28258)...	-	Oct 13, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 49324757 (NC_000006.12:49561026::TC 17813/28258) Row 49324758 (NC_000006.12:49561026::TCTC 73/28258) Row 49324759 (NC_000006.12:49561026:TC: 94/28258)...	-	Oct 13, 2022 (156)
112	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17776489 (NC_000006.11:49528739::TC 1724/3708) Row 17776490 (NC_000006.11:49528739:TC: 230/3708)	-	Oct 12, 2018 (152)
113	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17776489 (NC_000006.11:49528739::TC 1724/3708) Row 17776490 (NC_000006.11:49528739:TC: 230/3708)	-	Oct 12, 2018 (152)
114	ALFA	NC_000006.12 - 49561027	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)
rs140828140	Sep 17, 2011 (135)
rs904685146	Nov 08, 2017 (151)
rs72035538	May 15, 2013 (138)
rs150710871	May 11, 2012 (137)
rs796094024	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4141552880	NC_000006.12:49561026:TCTCTCTCTC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
ss4141552879, ss5268408674	NC_000006.12:49561026:TCTCTCTC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT	(self)
ss2999045232, ss5177455527	NC_000006.11:49528739:TCTCTC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
ss3959012617, ss4141552878, ss5715487656	NC_000006.12:49561026:TCTCTC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
ss5177455528	NC_000006.11:49528739:TCTC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3717188640, ss4141552877, ss5268408672, ss5715487657	NC_000006.12:49561026:TCTC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
ss1705158652, ss1705158709, ss5177455525, ss5842227481	NC_000006.11:49528739:TC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4141552876, ss5268408670, ss5466085414, ss5715487655	NC_000006.12:49561026:TC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3717188641	NC_000006.12:49561028:TC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3959012614	NC_000006.12:49561030:TC:	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss326802090, ss326849881, ss327097661, ss551614077, ss551797894, ss553247545	NC_000006.10:49636698::TC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss288722578	NC_000006.10:49636725::CT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
31876116, ss663700305, ss666353855, ss1375493257, ss1536503370, ss3733495069, ss3785471423, ss3790822846, ss3795701516, ss3829917681, ss3838436694, ss5177455524, ss5842227480	NC_000006.11:49528739::TC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss1710269560, ss1710269616	NC_000006.11:49528741::TC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3064204611, ss3065083448, ss3066080656, ss3808154496, ss3843881562, ss4141552871, ss5268408669, ss5466085413, ss5715487653, ss5855353523	NC_000006.12:49561026::TC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3717188642	NC_000006.12:49561030::TC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3959012613	NC_000006.12:49561032::TC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3648348694	NC_000006.12:49561049::CT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss42855415	NT_007592.15:49468739::TC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss82950155, ss95428164	NT_007592.15:49468766::CT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3733495071, ss5177455526	NC_000006.11:49528739::TCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4141552872, ss5268408671, ss5466085416, ss5715487654	NC_000006.12:49561026::TCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3717188643	NC_000006.12:49561030::TCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3959012615	NC_000006.12:49561032::TCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3733495070, ss5177455529	NC_000006.11:49528739::TCTCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4141552873, ss5268408673, ss5466085415, ss5715487658	NC_000006.12:49561026::TCTCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3717188644	NC_000006.12:49561030::TCTCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3959012616	NC_000006.12:49561032::TCTCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4141552874	NC_000006.12:49561026::TCTCTCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4141552875	NC_000006.12:49561026::TCTCTCTCTCTC	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
8008784405	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000006.12:49561026:TCTCTCTCTCTC… NC_000006.12:49561026:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(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 rs36182126

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs36182126