Name: rs60851148
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.

rs60851148

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:56220019-56220059 (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(AATA)₄ / del(AATA)₃ / del(AATA…
del(AATA)₄ / del(AATA)₃ / del(AATA)₂ / delAATA / dupAATA / dup(AATA)₂ / dup(AATA)₃ / dup(AATA)₄ / dup(AATA)₅
Variation Type: Indel Insertion and Deletion
Frequency: (AAAT)₁₀A=0.3417 (1711/5008, 1000G)
(AAAT)₁₀A=0.2082 (1010/4850, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RNF41 : Intron Variant
NABP2 : 2KB Upstream 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	4850	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.2082	AAATAAATAAATAAATAAATAAATA=0.0004, AAATAAATAAATAAATAAATAAATAAATA=0.0000, AAATAAATAAATAAATAAATAAATAAATAAATA=0.0004, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0427, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.7091, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0377, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0014, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0000	0.12818	0.659002	0.212818	32
European	Sub	4538	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.1556	AAATAAATAAATAAATAAATAAATA=0.0004, AAATAAATAAATAAATAAATAAATAAATA=0.0000, AAATAAATAAATAAATAAATAAATAAATAAATA=0.0004, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0454, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.7563, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0403, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0015, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0000	0.058232	0.711488	0.230281	32
African	Sub	258	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=1.000	AAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=1.0	AAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0	1.0	0.0	0.0	N/A
African American	Sub	250	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=1.000	AAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=1.0	AAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=1.0	AAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0	AAATAAATAAATAAATAAATAAATA=0, AAATAAATAAATAAATAAATAAATAAATA=0, AAATAAATAAATAAATAAATAAATAAATAAATA=0, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0	0	0	0	N/A
Latin American 1	Sub	2	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=1.0	AAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	10	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=1.0	AAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	8	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=1.0	AAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.0	1.0	0.0	0.0	N/A
Other	Sub	32	AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.75	AAATAAATAAATAAATAAATAAATA=0.00, AAATAAATAAATAAATAAATAAATAAATA=0.00, AAATAAATAAATAAATAAATAAATAAATAAATA=0.00, AAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.03, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.22, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.00, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.00, AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA=0.00	0.8	0.2	0.0	9

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupAATA=0.6583
1000Genomes	African	Sub	1322	- No frequency provided	dupAATA=0.2965
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupAATA=0.8383
1000Genomes	Europe	Sub	1006	- No frequency provided	dupAATA=0.8419
1000Genomes	South Asian	Sub	978	- No frequency provided	dupAATA=0.645
1000Genomes	American	Sub	694	- No frequency provided	dupAATA=0.839
Allele Frequency Aggregator	Total	Global	4850	(AAAT)₁₀A=0.2082	del(AATA)₄=0.0004, del(AATA)₃=0.0000, del(AATA)₂=0.0004, delAATA=0.0427, dupAATA=0.7091, dup(AATA)₂=0.0377, dup(AATA)₃=0.0014, dup(AATA)₄=0.0000
Allele Frequency Aggregator	European	Sub	4538	(AAAT)₁₀A=0.1556	del(AATA)₄=0.0004, del(AATA)₃=0.0000, del(AATA)₂=0.0004, delAATA=0.0454, dupAATA=0.7563, dup(AATA)₂=0.0403, dup(AATA)₃=0.0015, dup(AATA)₄=0.0000
Allele Frequency Aggregator	African	Sub	258	(AAAT)₁₀A=1.000	del(AATA)₄=0.000, del(AATA)₃=0.000, del(AATA)₂=0.000, delAATA=0.000, dupAATA=0.000, dup(AATA)₂=0.000, dup(AATA)₃=0.000, dup(AATA)₄=0.000
Allele Frequency Aggregator	Other	Sub	32	(AAAT)₁₀A=0.75	del(AATA)₄=0.00, del(AATA)₃=0.00, del(AATA)₂=0.00, delAATA=0.03, dupAATA=0.22, dup(AATA)₂=0.00, dup(AATA)₃=0.00, dup(AATA)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	10	(AAAT)₁₀A=1.0	del(AATA)₄=0.0, del(AATA)₃=0.0, del(AATA)₂=0.0, delAATA=0.0, dupAATA=0.0, dup(AATA)₂=0.0, dup(AATA)₃=0.0, dup(AATA)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	8	(AAAT)₁₀A=1.0	del(AATA)₄=0.0, del(AATA)₃=0.0, del(AATA)₂=0.0, delAATA=0.0, dupAATA=0.0, dup(AATA)₂=0.0, dup(AATA)₃=0.0, dup(AATA)₄=0.0
Allele Frequency Aggregator	Latin American 1	Sub	2	(AAAT)₁₀A=1.0	del(AATA)₄=0.0, del(AATA)₃=0.0, del(AATA)₂=0.0, delAATA=0.0, dupAATA=0.0, dup(AATA)₂=0.0, dup(AATA)₃=0.0, dup(AATA)₄=0.0
Allele Frequency Aggregator	Asian	Sub	2	(AAAT)₁₀A=1.0	del(AATA)₄=0.0, del(AATA)₃=0.0, del(AATA)₂=0.0, delAATA=0.0, dupAATA=0.0, dup(AATA)₂=0.0, dup(AATA)₃=0.0, dup(AATA)₄=0.0

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 12	NC_000012.12:g.56220020AATA[6]
GRCh38.p14 chr 12	NC_000012.12:g.56220020AATA[7]
GRCh38.p14 chr 12	NC_000012.12:g.56220020AATA[8]
GRCh38.p14 chr 12	NC_000012.12:g.56220020AATA[9]
GRCh38.p14 chr 12	NC_000012.12:g.56220020AATA[11]
GRCh38.p14 chr 12	NC_000012.12:g.56220020AATA[12]
GRCh38.p14 chr 12	NC_000012.12:g.56220020AATA[13]
GRCh38.p14 chr 12	NC_000012.12:g.56220020AATA[14]
GRCh38.p14 chr 12	NC_000012.12:g.56220020AATA[15]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[6]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[7]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[8]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[9]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[11]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[12]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[13]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[14]
GRCh37.p13 chr 12	NC_000012.11:g.56613804AATA[15]

Gene: RNF41, ring finger protein 41 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RNF41 transcript variant 4	NM_001242826.2:c.-209+153… NM_001242826.2:c.-209+1533ATTT[6]	N/A	Intron Variant
RNF41 transcript variant 1	NM_005785.4:c.-209+1702AT… NM_005785.4:c.-209+1702ATTT[6]	N/A	Intron Variant
RNF41 transcript variant 2	NM_194358.3:c.-565+1702AT… NM_194358.3:c.-565+1702ATTT[6]	N/A	Intron Variant
RNF41 transcript variant 3	NM_194359.2:c.-209+1845AT… NM_194359.2:c.-209+1845ATTT[6]	N/A	Intron Variant
RNF41 transcript variant 5	NR_040053.2:n.	N/A	Intron Variant
RNF41 transcript variant X1	XM_047428054.1:c.-209+170… XM_047428054.1:c.-209+1702ATTT[6]	N/A	Intron Variant

Gene: NABP2, nucleic acid binding protein 2 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
NABP2 transcript	NM_024068.4:c.	N/A	N/A
NABP2 transcript variant X3	XM_005269149.6:c.	N/A	Upstream Transcript Variant
NABP2 transcript variant X5	XM_047429533.1:c.	N/A	Upstream Transcript Variant
NABP2 transcript variant X2	XM_005269147.4:c.	N/A	N/A
NABP2 transcript variant X1	XM_047429531.1:c.	N/A	N/A
NABP2 transcript variant X4	XM_047429532.1:c.	N/A	N/A

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	(AAAT)₁₀A=	del(AATA)₄	del(AATA)₃	del(AATA)₂	delAATA	dupAATA	dup(AATA)₂	dup(AATA)₃	dup(AATA)₄	dup(AATA)₅
GRCh38.p14 chr 12	NC_000012.12:g.56220019_56220059=	NC_000012.12:g.56220020AATA[6]	NC_000012.12:g.56220020AATA[7]	NC_000012.12:g.56220020AATA[8]	NC_000012.12:g.56220020AATA[9]	NC_000012.12:g.56220020AATA[11]	NC_000012.12:g.56220020AATA[12]	NC_000012.12:g.56220020AATA[13]	NC_000012.12:g.56220020AATA[14]	NC_000012.12:g.56220020AATA[15]
GRCh37.p13 chr 12	NC_000012.11:g.56613803_56613843=	NC_000012.11:g.56613804AATA[6]	NC_000012.11:g.56613804AATA[7]	NC_000012.11:g.56613804AATA[8]	NC_000012.11:g.56613804AATA[9]	NC_000012.11:g.56613804AATA[11]	NC_000012.11:g.56613804AATA[12]	NC_000012.11:g.56613804AATA[13]	NC_000012.11:g.56613804AATA[14]	NC_000012.11:g.56613804AATA[15]
RNF41 transcript variant 4	NM_001242826.1:c.-209+1572=	NM_001242826.1:c.-209+1533ATTT[6]	NM_001242826.1:c.-209+1533ATTT[7]	NM_001242826.1:c.-209+1533ATTT[8]	NM_001242826.1:c.-209+1533ATTT[9]	NM_001242826.1:c.-209+1533ATTT[11]	NM_001242826.1:c.-209+1533ATTT[12]	NM_001242826.1:c.-209+1533ATTT[13]	NM_001242826.1:c.-209+1533ATTT[14]	NM_001242826.1:c.-209+1533ATTT[15]
RNF41 transcript variant 4	NM_001242826.2:c.-209+1572=	NM_001242826.2:c.-209+1533ATTT[6]	NM_001242826.2:c.-209+1533ATTT[7]	NM_001242826.2:c.-209+1533ATTT[8]	NM_001242826.2:c.-209+1533ATTT[9]	NM_001242826.2:c.-209+1533ATTT[11]	NM_001242826.2:c.-209+1533ATTT[12]	NM_001242826.2:c.-209+1533ATTT[13]	NM_001242826.2:c.-209+1533ATTT[14]	NM_001242826.2:c.-209+1533ATTT[15]
RNF41 transcript variant 1	NM_005785.3:c.-209+1741=	NM_005785.3:c.-209+1702ATTT[6]	NM_005785.3:c.-209+1702ATTT[7]	NM_005785.3:c.-209+1702ATTT[8]	NM_005785.3:c.-209+1702ATTT[9]	NM_005785.3:c.-209+1702ATTT[11]	NM_005785.3:c.-209+1702ATTT[12]	NM_005785.3:c.-209+1702ATTT[13]	NM_005785.3:c.-209+1702ATTT[14]	NM_005785.3:c.-209+1702ATTT[15]
RNF41 transcript variant 1	NM_005785.4:c.-209+1741=	NM_005785.4:c.-209+1702ATTT[6]	NM_005785.4:c.-209+1702ATTT[7]	NM_005785.4:c.-209+1702ATTT[8]	NM_005785.4:c.-209+1702ATTT[9]	NM_005785.4:c.-209+1702ATTT[11]	NM_005785.4:c.-209+1702ATTT[12]	NM_005785.4:c.-209+1702ATTT[13]	NM_005785.4:c.-209+1702ATTT[14]	NM_005785.4:c.-209+1702ATTT[15]
RNF41 transcript variant 2	NM_194358.2:c.-565+1741=	NM_194358.2:c.-565+1702ATTT[6]	NM_194358.2:c.-565+1702ATTT[7]	NM_194358.2:c.-565+1702ATTT[8]	NM_194358.2:c.-565+1702ATTT[9]	NM_194358.2:c.-565+1702ATTT[11]	NM_194358.2:c.-565+1702ATTT[12]	NM_194358.2:c.-565+1702ATTT[13]	NM_194358.2:c.-565+1702ATTT[14]	NM_194358.2:c.-565+1702ATTT[15]
RNF41 transcript variant 2	NM_194358.3:c.-565+1741=	NM_194358.3:c.-565+1702ATTT[6]	NM_194358.3:c.-565+1702ATTT[7]	NM_194358.3:c.-565+1702ATTT[8]	NM_194358.3:c.-565+1702ATTT[9]	NM_194358.3:c.-565+1702ATTT[11]	NM_194358.3:c.-565+1702ATTT[12]	NM_194358.3:c.-565+1702ATTT[13]	NM_194358.3:c.-565+1702ATTT[14]	NM_194358.3:c.-565+1702ATTT[15]
RNF41 transcript variant 3	NM_194359.2:c.-209+1884=	NM_194359.2:c.-209+1845ATTT[6]	NM_194359.2:c.-209+1845ATTT[7]	NM_194359.2:c.-209+1845ATTT[8]	NM_194359.2:c.-209+1845ATTT[9]	NM_194359.2:c.-209+1845ATTT[11]	NM_194359.2:c.-209+1845ATTT[12]	NM_194359.2:c.-209+1845ATTT[13]	NM_194359.2:c.-209+1845ATTT[14]	NM_194359.2:c.-209+1845ATTT[15]
RNF41 transcript variant X1	XM_005268561.1:c.-565+1884=	XM_005268561.1:c.-565+1845ATTT[6]	XM_005268561.1:c.-565+1845ATTT[7]	XM_005268561.1:c.-565+1845ATTT[8]	XM_005268561.1:c.-565+1845ATTT[9]	XM_005268561.1:c.-565+1845ATTT[11]	XM_005268561.1:c.-565+1845ATTT[12]	XM_005268561.1:c.-565+1845ATTT[13]	XM_005268561.1:c.-565+1845ATTT[14]	XM_005268561.1:c.-565+1845ATTT[15]
RNF41 transcript variant X1	XM_047428054.1:c.-209+1741=	XM_047428054.1:c.-209+1702ATTT[6]	XM_047428054.1:c.-209+1702ATTT[7]	XM_047428054.1:c.-209+1702ATTT[8]	XM_047428054.1:c.-209+1702ATTT[9]	XM_047428054.1:c.-209+1702ATTT[11]	XM_047428054.1:c.-209+1702ATTT[12]	XM_047428054.1:c.-209+1702ATTT[13]	XM_047428054.1:c.-209+1702ATTT[14]	XM_047428054.1:c.-209+1702ATTT[15]

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#.

74 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80929997	Dec 04, 2013 (138)
2	HUMANGENOME_JCVI	ss95597534	Feb 06, 2009 (130)
3	GMI	ss289130257	May 04, 2012 (137)
4	1000GENOMES	ss327980203	Jan 10, 2018 (151)
5	LUNTER	ss552218400	Apr 25, 2013 (138)
6	LUNTER	ss552498164	Apr 25, 2013 (138)
7	LUNTER	ss553487881	Apr 25, 2013 (138)
8	SSMP	ss664128962	Apr 01, 2015 (144)
9	BILGI_BIOE	ss666570761	Apr 25, 2013 (138)
10	1000GENOMES	ss1372202474	Aug 21, 2014 (142)
11	DDI	ss1536728215	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1707479247	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1707479385	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1710561527	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1710561528	Apr 01, 2015 (144)
16	SWEGEN	ss3009743224	Nov 08, 2017 (151)
17	MCHAISSO	ss3063731099	Jan 10, 2018 (151)
18	MCHAISSO	ss3064560463	Nov 08, 2017 (151)
19	MCHAISSO	ss3065478241	Nov 08, 2017 (151)
20	EVA_DECODE	ss3693734117	Jul 13, 2019 (153)
21	EVA_DECODE	ss3693734118	Jul 13, 2019 (153)
22	EVA_DECODE	ss3693734119	Jul 13, 2019 (153)
23	EVA_DECODE	ss3693734120	Jul 13, 2019 (153)
24	ACPOP	ss3739050123	Jul 13, 2019 (153)
25	ACPOP	ss3739050124	Jul 13, 2019 (153)
26	ACPOP	ss3739050125	Jul 13, 2019 (153)
27	ACPOP	ss3739050126	Jul 13, 2019 (153)
28	PACBIO	ss3787235507	Jul 13, 2019 (153)
29	PACBIO	ss3787235508	Jul 13, 2019 (153)
30	PACBIO	ss3792335484	Jul 13, 2019 (153)
31	PACBIO	ss3792335485	Jul 13, 2019 (153)
32	PACBIO	ss3797218250	Jul 13, 2019 (153)
33	PACBIO	ss3797218251	Jul 13, 2019 (153)
34	KHV_HUMAN_GENOMES	ss3815849081	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3815849082	Jul 13, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3815849083	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3815849084	Jul 13, 2019 (153)
38	KHV_HUMAN_GENOMES	ss3815849085	Jul 13, 2019 (153)
39	EVA	ss3833139455	Apr 27, 2020 (154)
40	EVA	ss3845625943	Apr 27, 2020 (154)
41	GNOMAD	ss4252373706	Apr 26, 2021 (155)
42	GNOMAD	ss4252373707	Apr 26, 2021 (155)
43	GNOMAD	ss4252373708	Apr 26, 2021 (155)
44	GNOMAD	ss4252373709	Apr 26, 2021 (155)
45	GNOMAD	ss4252373710	Apr 26, 2021 (155)
46	GNOMAD	ss4252373712	Apr 26, 2021 (155)
47	GNOMAD	ss4252373713	Apr 26, 2021 (155)
48	GNOMAD	ss4252373714	Apr 26, 2021 (155)
49	GNOMAD	ss4252373715	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5206474422	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5206474423	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5206474424	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5206474425	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5206474426	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5206474427	Apr 26, 2021 (155)
56	1000G_HIGH_COVERAGE	ss5290925239	Oct 16, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5290925240	Oct 16, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5290925241	Oct 16, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5290925242	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5290925243	Oct 16, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5290925244	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5485663093	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5485663094	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5485663095	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5485663096	Oct 16, 2022 (156)
66	HUGCELL_USP	ss5485663097	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5756312738	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5756312739	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5756312740	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5756312741	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5756312742	Oct 16, 2022 (156)
72	TOMMO_GENOMICS	ss5756312743	Oct 16, 2022 (156)
73	EVA	ss5838009575	Oct 16, 2022 (156)
74	EVA	ss5838009576	Oct 16, 2022 (156)
75	1000Genomes	NC_000012.11 - 56613803	Oct 12, 2018 (152)
76	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32146330 (NC_000012.11:56613802::AAAT 3379/3854) Row 32146331 (NC_000012.11:56613802:AAAT: 210/3854)	-	Oct 12, 2018 (152)
77	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32146330 (NC_000012.11:56613802::AAAT 3379/3854) Row 32146331 (NC_000012.11:56613802:AAAT: 210/3854)	-	Oct 12, 2018 (152)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408293025 (NC_000012.12:56220018::AAAT 82620/127908) Row 408293026 (NC_000012.12:56220018::AAATAAAT 5632/128044) Row 408293027 (NC_000012.12:56220018::AAATAAATAAAT 164/128136)...	-	Apr 26, 2021 (155)
87	Northern Sweden Submission ignored due to conflicting rows: Row 12334988 (NC_000012.11:56613802::AAAT 512/600) Row 12334989 (NC_000012.11:56613802:AAAT: 39/600) Row 12334990 (NC_000012.11:56613802::AAATAAAT 18/600)...	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 12334988 (NC_000012.11:56613802::AAAT 512/600) Row 12334989 (NC_000012.11:56613802:AAAT: 39/600) Row 12334990 (NC_000012.11:56613802::AAATAAAT 18/600)...	-	Jul 13, 2019 (153)
89	Northern Sweden Submission ignored due to conflicting rows: Row 12334988 (NC_000012.11:56613802::AAAT 512/600) Row 12334989 (NC_000012.11:56613802:AAAT: 39/600) Row 12334990 (NC_000012.11:56613802::AAATAAAT 18/600)...	-	Jul 13, 2019 (153)
90	Northern Sweden Submission ignored due to conflicting rows: Row 12334988 (NC_000012.11:56613802::AAAT 512/600) Row 12334989 (NC_000012.11:56613802:AAAT: 39/600) Row 12334990 (NC_000012.11:56613802::AAATAAAT 18/600)...	-	Jul 13, 2019 (153)
91	8.3KJPN Submission ignored due to conflicting rows: Row 64443729 (NC_000012.11:56613802::AAAT 11916/16752) Row 64443730 (NC_000012.11:56613802::AAATAAAT 394/16752) Row 64443731 (NC_000012.11:56613802:AAAT: 78/16752)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 64443729 (NC_000012.11:56613802::AAAT 11916/16752) Row 64443730 (NC_000012.11:56613802::AAATAAAT 394/16752) Row 64443731 (NC_000012.11:56613802:AAAT: 78/16752)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 64443729 (NC_000012.11:56613802::AAAT 11916/16752) Row 64443730 (NC_000012.11:56613802::AAATAAAT 394/16752) Row 64443731 (NC_000012.11:56613802:AAAT: 78/16752)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 64443729 (NC_000012.11:56613802::AAAT 11916/16752) Row 64443730 (NC_000012.11:56613802::AAATAAAT 394/16752) Row 64443731 (NC_000012.11:56613802:AAAT: 78/16752)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 64443729 (NC_000012.11:56613802::AAAT 11916/16752) Row 64443730 (NC_000012.11:56613802::AAATAAAT 394/16752) Row 64443731 (NC_000012.11:56613802:AAAT: 78/16752)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 64443729 (NC_000012.11:56613802::AAAT 11916/16752) Row 64443730 (NC_000012.11:56613802::AAATAAAT 394/16752) Row 64443731 (NC_000012.11:56613802:AAAT: 78/16752)...	-	Apr 26, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 90149842 (NC_000012.12:56220018::AAAT 20072/28258) Row 90149843 (NC_000012.12:56220018::AAATAAAT 677/28258) Row 90149844 (NC_000012.12:56220018:AAATAAAT: 167/28258)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 90149842 (NC_000012.12:56220018::AAAT 20072/28258) Row 90149843 (NC_000012.12:56220018::AAATAAAT 677/28258) Row 90149844 (NC_000012.12:56220018:AAATAAAT: 167/28258)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 90149842 (NC_000012.12:56220018::AAAT 20072/28258) Row 90149843 (NC_000012.12:56220018::AAATAAAT 677/28258) Row 90149844 (NC_000012.12:56220018:AAATAAAT: 167/28258)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 90149842 (NC_000012.12:56220018::AAAT 20072/28258) Row 90149843 (NC_000012.12:56220018::AAATAAAT 677/28258) Row 90149844 (NC_000012.12:56220018:AAATAAAT: 167/28258)...	-	Oct 16, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 90149842 (NC_000012.12:56220018::AAAT 20072/28258) Row 90149843 (NC_000012.12:56220018::AAATAAAT 677/28258) Row 90149844 (NC_000012.12:56220018:AAATAAAT: 167/28258)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 90149842 (NC_000012.12:56220018::AAAT 20072/28258) Row 90149843 (NC_000012.12:56220018::AAATAAAT 677/28258) Row 90149844 (NC_000012.12:56220018:AAATAAAT: 167/28258)...	-	Oct 16, 2022 (156)
103	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32146330 (NC_000012.11:56613802::AAAT 3345/3708) Row 32146331 (NC_000012.11:56613802:AAAT: 169/3708)	-	Oct 12, 2018 (152)
104	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32146330 (NC_000012.11:56613802::AAAT 3345/3708) Row 32146331 (NC_000012.11:56613802:AAAT: 169/3708)	-	Oct 12, 2018 (152)
105	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7135982 (NC_000012.11:56613802::AAATAAAT 5/55) Row 7135983 (NC_000012.11:56613802:AAAT: 3/53) Row 7135984 (NC_000012.11:56613802:AAATAAAT: 2/52)...	-	Jul 13, 2019 (153)
106	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7135982 (NC_000012.11:56613802::AAATAAAT 5/55) Row 7135983 (NC_000012.11:56613802:AAAT: 3/53) Row 7135984 (NC_000012.11:56613802:AAATAAAT: 2/52)...	-	Jul 13, 2019 (153)
107	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7135982 (NC_000012.11:56613802::AAATAAAT 5/55) Row 7135983 (NC_000012.11:56613802:AAAT: 3/53) Row 7135984 (NC_000012.11:56613802:AAATAAAT: 2/52)...	-	Jul 13, 2019 (153)
108	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7135982 (NC_000012.11:56613802::AAATAAAT 5/55) Row 7135983 (NC_000012.11:56613802:AAAT: 3/53) Row 7135984 (NC_000012.11:56613802:AAATAAAT: 2/52)...	-	Jul 13, 2019 (153)
109	ALFA	NC_000012.12 - 56220019	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)
rs71979549	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3009743224, ss3739050126, ss5206474426	NC_000012.11:56613802:AAATAAATAAAT… NC_000012.11:56613802:AAATAAATAAATAAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATA	(self)
ss4252373715	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATA	(self)
2558772850	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATA	(self)
ss4252373714, ss5290925243, ss5485663097, ss5756312743	NC_000012.12:56220018:AAATAAATAAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATA	(self)
2558772850	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATA	(self)
ss5206474425	NC_000012.11:56613802:AAATAAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss3693734120, ss3815849083, ss4252373713, ss5290925242, ss5485663096, ss5756312740	NC_000012.12:56220018:AAATAAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATA	(self)
2558772850	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss327980203, ss552498164	NC_000012.10:54900069:AAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss1707479247, ss1707479385, ss3739050124, ss5206474424, ss5838009576	NC_000012.11:56613802:AAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss3064560463, ss3065478241, ss4252373712, ss5290925241, ss5485663095, ss5756312741	NC_000012.12:56220018:AAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
2558772850	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss3693734119, ss3815849082	NC_000012.12:56220022:AAAT:	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss552218400, ss553487881	NC_000012.10:54900069::AAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss289130257	NC_000012.10:54900110::AATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
57898381, ss664128962, ss666570761, ss1372202474, ss1536728215, ss3739050123, ss3787235507, ss3792335484, ss3797218250, ss3833139455, ss5206474422, ss5838009575	NC_000012.11:56613802::AAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss1710561527, ss1710561528	NC_000012.11:56613806::AAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss3063731099, ss3815849084, ss3845625943, ss4252373706, ss5290925240, ss5485663093, ss5756312738	NC_000012.12:56220018::AAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
2558772850	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss3693734118, ss3815849081	NC_000012.12:56220026::AAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss80929997, ss95597534	NT_029419.12:18757149::AATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss3739050125, ss3787235508, ss3792335485, ss3797218251, ss5206474423	NC_000012.11:56613802::AAATAAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss4252373707, ss5290925239, ss5485663094, ss5756312739	NC_000012.12:56220018::AAATAAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
2558772850	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss3693734117, ss3815849085	NC_000012.12:56220026::AAATAAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss5206474427	NC_000012.11:56613802::AAATAAATAAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss4252373708, ss5290925244, ss5756312742	NC_000012.12:56220018::AAATAAATAAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
2558772850	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss4252373709	NC_000012.12:56220018::AAATAAATAAA… NC_000012.12:56220018::AAATAAATAAATAAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
2558772850	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(self)
ss4252373710	NC_000012.12:56220018::AAATAAATAAA… NC_000012.12:56220018::AAATAAATAAATAAATAAAT	NC_000012.12:56220018:AAATAAATAAAT… NC_000012.12:56220018:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA:AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATA	(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 rs60851148

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

rs60851148