Name: rs140524601
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.

rs140524601

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:68296565-68296581 (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(GT)₄ / del(GT)₃ / delGTGT / de…
del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₇ / dup(GT)₈ / ins(GT)₉
Variation Type: Indel Insertion and Deletion
Frequency: dupGTGT=0.2080 (1400/6730, ALFA)
(TG)₈T=0.4159 (2083/5008, 1000G)
(TG)₈T=0.4 (3/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CNRIP1 : Intron Variant
LOC107985892 : 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	6730	TGTGTGTGTGTGTGTGT=0.6505	TGTGTGTGT=0.0000, TGTGTGTGTGT=0.0000, TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0012, TGTGTGTGTGTGTGTGTGTGT=0.2080, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0498, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0860, TGTGTGTGTGTGTGTGTGTGTGT=0.0033, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0012, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.648767	0.085521	0.265712	32
European	Sub	5768	TGTGTGTGTGTGTGTGT=0.5931	TGTGTGTGT=0.0000, TGTGTGTGTGT=0.0000, TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0014, TGTGTGTGTGTGTGTGTGTGT=0.2420, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0581, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1002, TGTGTGTGTGTGTGTGTGTGTGT=0.0038, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0014, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.567355	0.105703	0.326942	31
African	Sub	706	TGTGTGTGTGTGTGTGT=1.000	TGTGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	36	TGTGTGTGTGTGTGTGT=1.00	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	670	TGTGTGTGTGTGTGTGT=1.000	TGTGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	TGTGTGTGTGTGTGTGT=1.0	TGTGTGTGT=0.0, TGTGTGTGTGT=0.0, TGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	TGTGTGTGTGTGTGTGT=1.0	TGTGTGTGT=0.0, TGTGTGTGTGT=0.0, TGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TGTGTGTGTGTGTGTGT=0	TGTGTGTGT=0, TGTGTGTGTGT=0, TGTGTGTGTGTGT=0, TGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Latin American 1	Sub	16	TGTGTGTGTGTGTGTGT=1.00	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	138	TGTGTGTGTGTGTGTGT=1.000	TGTGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	24	TGTGTGTGTGTGTGTGT=1.00	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	72	TGTGTGTGTGTGTGTGT=0.93	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.06, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.01, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	0.914286	0.0	0.085714	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	6730	(TG)₈T=0.6505	del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.0012, dupGTGT=0.2080, dup(GT)₃=0.0033, dup(GT)₄=0.0000, dup(GT)₅=0.0498, dup(GT)₆=0.0860, dup(GT)₇=0.0012, dup(GT)₈=0.0000, ins(GT)₉=0.0000
Allele Frequency Aggregator	European	Sub	5768	(TG)₈T=0.5931	del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.0014, dupGTGT=0.2420, dup(GT)₃=0.0038, dup(GT)₄=0.0000, dup(GT)₅=0.0581, dup(GT)₆=0.1002, dup(GT)₇=0.0014, dup(GT)₈=0.0000, ins(GT)₉=0.0000
Allele Frequency Aggregator	African	Sub	706	(TG)₈T=1.000	del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, ins(GT)₉=0.000
Allele Frequency Aggregator	Latin American 2	Sub	138	(TG)₈T=1.000	del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, ins(GT)₉=0.000
Allele Frequency Aggregator	Other	Sub	72	(TG)₈T=0.93	del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.06, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.01, dup(GT)₇=0.00, dup(GT)₈=0.00, ins(GT)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(TG)₈T=1.00	del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, ins(GT)₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(TG)₈T=1.00	del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, ins(GT)₉=0.00
Allele Frequency Aggregator	Asian	Sub	6	(TG)₈T=1.0	del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0, dup(GT)₆=0.0, dup(GT)₇=0.0, dup(GT)₈=0.0, ins(GT)₉=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupGTGT=0.4732, dup(GT)₅=0.1108
1000Genomes	African	Sub	1322	- No frequency provided	dupGTGT=0.3464, dup(GT)₅=0.1483
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupGTGT=0.6815, dup(GT)₅=0.0079
1000Genomes	Europe	Sub	1006	- No frequency provided	dupGTGT=0.4066, dup(GT)₅=0.1213
1000Genomes	South Asian	Sub	978	- No frequency provided	dupGTGT=0.525, dup(GT)₅=0.177
1000Genomes	American	Sub	694	- No frequency provided	dupGTGT=0.437, dup(GT)₅=0.081
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupGTGT=0.6

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 2	NC_000002.12:g.68296566GT[4]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[5]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[6]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[7]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[9]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[10]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[11]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[12]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[13]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[14]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[15]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[16]
GRCh38.p14 chr 2	NC_000002.12:g.68296566GT[17]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[4]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[5]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[6]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[7]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[9]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[10]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[11]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[12]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[13]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[14]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[15]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[16]
GRCh37.p13 chr 2	NC_000002.11:g.68523698GT[17]

Gene: CNRIP1, cannabinoid receptor interacting protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CNRIP1 transcript variant 2	NM_001111101.2:c.331-1209… NM_001111101.2:c.331-12096CA[4]	N/A	Intron Variant
CNRIP1 transcript variant 3	NM_001371604.1:c.331-2554… NM_001371604.1:c.331-2554CA[4]	N/A	Intron Variant
CNRIP1 transcript variant 4	NM_001371605.1:c.331-2554… NM_001371605.1:c.331-2554CA[4]	N/A	Intron Variant
CNRIP1 transcript variant 5	NM_001371606.1:c.331-2554… NM_001371606.1:c.331-2554CA[4]	N/A	Intron Variant
CNRIP1 transcript variant 6	NM_001371607.1:c.244-2554… NM_001371607.1:c.244-2554CA[4]	N/A	Intron Variant
CNRIP1 transcript variant 7	NM_001371608.1:c.244-2554… NM_001371608.1:c.244-2554CA[4]	N/A	Intron Variant
CNRIP1 transcript variant 1	NM_015463.3:c.331-2554CA[… NM_015463.3:c.331-2554CA[4]	N/A	Intron Variant
CNRIP1 transcript variant 8	NR_163969.1:n.	N/A	Intron Variant
CNRIP1 transcript variant 9	NR_163970.1:n.	N/A	Intron Variant
CNRIP1 transcript variant 10	NR_163971.1:n.	N/A	Intron Variant

Gene: LOC107985892, uncharacterized LOC107985892 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107985892 transcript variant X2	XR_001739526.2:n.	N/A	Intron Variant
LOC107985892 transcript variant X1	XR_001739527.2: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	(TG)₈T=	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₇	dup(GT)₈	ins(GT)₉
GRCh38.p14 chr 2	NC_000002.12:g.68296565_68296581=	NC_000002.12:g.68296566GT[4]	NC_000002.12:g.68296566GT[5]	NC_000002.12:g.68296566GT[6]	NC_000002.12:g.68296566GT[7]	NC_000002.12:g.68296566GT[9]	NC_000002.12:g.68296566GT[10]	NC_000002.12:g.68296566GT[11]	NC_000002.12:g.68296566GT[12]	NC_000002.12:g.68296566GT[13]	NC_000002.12:g.68296566GT[14]	NC_000002.12:g.68296566GT[15]	NC_000002.12:g.68296566GT[16]	NC_000002.12:g.68296566GT[17]
GRCh37.p13 chr 2	NC_000002.11:g.68523697_68523713=	NC_000002.11:g.68523698GT[4]	NC_000002.11:g.68523698GT[5]	NC_000002.11:g.68523698GT[6]	NC_000002.11:g.68523698GT[7]	NC_000002.11:g.68523698GT[9]	NC_000002.11:g.68523698GT[10]	NC_000002.11:g.68523698GT[11]	NC_000002.11:g.68523698GT[12]	NC_000002.11:g.68523698GT[13]	NC_000002.11:g.68523698GT[14]	NC_000002.11:g.68523698GT[15]	NC_000002.11:g.68523698GT[16]	NC_000002.11:g.68523698GT[17]
CNRIP1 transcript variant CRIP1b	NM_001111101.1:c.331-12081=	NM_001111101.1:c.331-12096CA[4]	NM_001111101.1:c.331-12096CA[5]	NM_001111101.1:c.331-12096CA[6]	NM_001111101.1:c.331-12096CA[7]	NM_001111101.1:c.331-12096CA[9]	NM_001111101.1:c.331-12096CA[10]	NM_001111101.1:c.331-12096CA[11]	NM_001111101.1:c.331-12096CA[12]	NM_001111101.1:c.331-12096CA[13]	NM_001111101.1:c.331-12096CA[14]	NM_001111101.1:c.331-12096CA[15]	NM_001111101.1:c.331-12096CA[16]	NM_001111101.1:c.331-12096CA[17]
CNRIP1 transcript variant 2	NM_001111101.2:c.331-12081=	NM_001111101.2:c.331-12096CA[4]	NM_001111101.2:c.331-12096CA[5]	NM_001111101.2:c.331-12096CA[6]	NM_001111101.2:c.331-12096CA[7]	NM_001111101.2:c.331-12096CA[9]	NM_001111101.2:c.331-12096CA[10]	NM_001111101.2:c.331-12096CA[11]	NM_001111101.2:c.331-12096CA[12]	NM_001111101.2:c.331-12096CA[13]	NM_001111101.2:c.331-12096CA[14]	NM_001111101.2:c.331-12096CA[15]	NM_001111101.2:c.331-12096CA[16]	NM_001111101.2:c.331-12096CA[17]
CNRIP1 transcript variant 3	NM_001371604.1:c.331-2539=	NM_001371604.1:c.331-2554CA[4]	NM_001371604.1:c.331-2554CA[5]	NM_001371604.1:c.331-2554CA[6]	NM_001371604.1:c.331-2554CA[7]	NM_001371604.1:c.331-2554CA[9]	NM_001371604.1:c.331-2554CA[10]	NM_001371604.1:c.331-2554CA[11]	NM_001371604.1:c.331-2554CA[12]	NM_001371604.1:c.331-2554CA[13]	NM_001371604.1:c.331-2554CA[14]	NM_001371604.1:c.331-2554CA[15]	NM_001371604.1:c.331-2554CA[16]	NM_001371604.1:c.331-2554CA[17]
CNRIP1 transcript variant 4	NM_001371605.1:c.331-2539=	NM_001371605.1:c.331-2554CA[4]	NM_001371605.1:c.331-2554CA[5]	NM_001371605.1:c.331-2554CA[6]	NM_001371605.1:c.331-2554CA[7]	NM_001371605.1:c.331-2554CA[9]	NM_001371605.1:c.331-2554CA[10]	NM_001371605.1:c.331-2554CA[11]	NM_001371605.1:c.331-2554CA[12]	NM_001371605.1:c.331-2554CA[13]	NM_001371605.1:c.331-2554CA[14]	NM_001371605.1:c.331-2554CA[15]	NM_001371605.1:c.331-2554CA[16]	NM_001371605.1:c.331-2554CA[17]
CNRIP1 transcript variant 5	NM_001371606.1:c.331-2539=	NM_001371606.1:c.331-2554CA[4]	NM_001371606.1:c.331-2554CA[5]	NM_001371606.1:c.331-2554CA[6]	NM_001371606.1:c.331-2554CA[7]	NM_001371606.1:c.331-2554CA[9]	NM_001371606.1:c.331-2554CA[10]	NM_001371606.1:c.331-2554CA[11]	NM_001371606.1:c.331-2554CA[12]	NM_001371606.1:c.331-2554CA[13]	NM_001371606.1:c.331-2554CA[14]	NM_001371606.1:c.331-2554CA[15]	NM_001371606.1:c.331-2554CA[16]	NM_001371606.1:c.331-2554CA[17]
CNRIP1 transcript variant 6	NM_001371607.1:c.244-2539=	NM_001371607.1:c.244-2554CA[4]	NM_001371607.1:c.244-2554CA[5]	NM_001371607.1:c.244-2554CA[6]	NM_001371607.1:c.244-2554CA[7]	NM_001371607.1:c.244-2554CA[9]	NM_001371607.1:c.244-2554CA[10]	NM_001371607.1:c.244-2554CA[11]	NM_001371607.1:c.244-2554CA[12]	NM_001371607.1:c.244-2554CA[13]	NM_001371607.1:c.244-2554CA[14]	NM_001371607.1:c.244-2554CA[15]	NM_001371607.1:c.244-2554CA[16]	NM_001371607.1:c.244-2554CA[17]
CNRIP1 transcript variant 7	NM_001371608.1:c.244-2539=	NM_001371608.1:c.244-2554CA[4]	NM_001371608.1:c.244-2554CA[5]	NM_001371608.1:c.244-2554CA[6]	NM_001371608.1:c.244-2554CA[7]	NM_001371608.1:c.244-2554CA[9]	NM_001371608.1:c.244-2554CA[10]	NM_001371608.1:c.244-2554CA[11]	NM_001371608.1:c.244-2554CA[12]	NM_001371608.1:c.244-2554CA[13]	NM_001371608.1:c.244-2554CA[14]	NM_001371608.1:c.244-2554CA[15]	NM_001371608.1:c.244-2554CA[16]	NM_001371608.1:c.244-2554CA[17]
CNRIP1 transcript variant CRIP1a	NM_015463.2:c.331-2539=	NM_015463.2:c.331-2554CA[4]	NM_015463.2:c.331-2554CA[5]	NM_015463.2:c.331-2554CA[6]	NM_015463.2:c.331-2554CA[7]	NM_015463.2:c.331-2554CA[9]	NM_015463.2:c.331-2554CA[10]	NM_015463.2:c.331-2554CA[11]	NM_015463.2:c.331-2554CA[12]	NM_015463.2:c.331-2554CA[13]	NM_015463.2:c.331-2554CA[14]	NM_015463.2:c.331-2554CA[15]	NM_015463.2:c.331-2554CA[16]	NM_015463.2:c.331-2554CA[17]
CNRIP1 transcript variant 1	NM_015463.3:c.331-2539=	NM_015463.3:c.331-2554CA[4]	NM_015463.3:c.331-2554CA[5]	NM_015463.3:c.331-2554CA[6]	NM_015463.3:c.331-2554CA[7]	NM_015463.3:c.331-2554CA[9]	NM_015463.3:c.331-2554CA[10]	NM_015463.3:c.331-2554CA[11]	NM_015463.3:c.331-2554CA[12]	NM_015463.3:c.331-2554CA[13]	NM_015463.3:c.331-2554CA[14]	NM_015463.3:c.331-2554CA[15]	NM_015463.3:c.331-2554CA[16]	NM_015463.3:c.331-2554CA[17]
CNRIP1 transcript variant X1	XM_005264249.1:c.331-2539=	XM_005264249.1:c.331-2554CA[4]	XM_005264249.1:c.331-2554CA[5]	XM_005264249.1:c.331-2554CA[6]	XM_005264249.1:c.331-2554CA[7]	XM_005264249.1:c.331-2554CA[9]	XM_005264249.1:c.331-2554CA[10]	XM_005264249.1:c.331-2554CA[11]	XM_005264249.1:c.331-2554CA[12]	XM_005264249.1:c.331-2554CA[13]	XM_005264249.1:c.331-2554CA[14]	XM_005264249.1:c.331-2554CA[15]	XM_005264249.1:c.331-2554CA[16]	XM_005264249.1:c.331-2554CA[17]

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#.

69 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95275760	Dec 05, 2013 (138)
2	GMI	ss288175703	Oct 11, 2018 (152)
3	1000GENOMES	ss326209777	May 09, 2011 (134)
4	1000GENOMES	ss326221726	May 09, 2011 (134)
5	1000GENOMES	ss326287134	May 09, 2011 (134)
6	LUNTER	ss551090392	Apr 25, 2013 (138)
7	LUNTER	ss551138127	Apr 25, 2013 (138)
8	LUNTER	ss552901267	Apr 25, 2013 (138)
9	SSMP	ss663322783	Apr 01, 2015 (144)
10	BILGI_BIOE	ss666151897	Apr 25, 2013 (138)
11	1000GENOMES	ss1368282687	Aug 21, 2014 (142)
12	1000GENOMES	ss1368282691	Aug 21, 2014 (142)
13	DDI	ss1536292569	Apr 01, 2015 (144)
14	SYSTEMSBIOZJU	ss2624822607	Nov 08, 2017 (151)
15	SWEGEN	ss2989687231	Nov 08, 2017 (151)
16	SWEGEN	ss2989687232	Nov 08, 2017 (151)
17	SWEGEN	ss2989687233	Nov 08, 2017 (151)
18	SWEGEN	ss2989687234	Nov 08, 2017 (151)
19	SWEGEN	ss2989687235	Nov 08, 2017 (151)
20	SWEGEN	ss2989687236	Nov 08, 2017 (151)
21	MCHAISSO	ss3063940644	Nov 08, 2017 (151)
22	MCHAISSO	ss3064791778	Nov 08, 2017 (151)
23	MCHAISSO	ss3065746023	Nov 08, 2017 (151)
24	URBANLAB	ss3647056987	Oct 11, 2018 (152)
25	PACBIO	ss3783891359	Jul 13, 2019 (153)
26	PACBIO	ss3789473696	Jul 13, 2019 (153)
27	PACBIO	ss3794346639	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3801265090	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3801265091	Jul 13, 2019 (153)
30	EVA	ss3827036939	Apr 25, 2020 (154)
31	EVA	ss3836928092	Apr 25, 2020 (154)
32	EVA	ss3842344053	Apr 25, 2020 (154)
33	KRGDB	ss3897935312	Apr 25, 2020 (154)
34	GNOMAD	ss4043288992	Apr 25, 2021 (155)
35	GNOMAD	ss4043288993	Apr 25, 2021 (155)
36	GNOMAD	ss4043288995	Apr 25, 2021 (155)
37	GNOMAD	ss4043288996	Apr 25, 2021 (155)
38	GNOMAD	ss4043288997	Apr 25, 2021 (155)
39	GNOMAD	ss4043288998	Apr 25, 2021 (155)
40	GNOMAD	ss4043288999	Apr 25, 2021 (155)
41	GNOMAD	ss4043289000	Apr 25, 2021 (155)
42	GNOMAD	ss4043289001	Apr 25, 2021 (155)
43	GNOMAD	ss4043289004	Apr 25, 2021 (155)
44	GNOMAD	ss4043289005	Apr 25, 2021 (155)
45	GNOMAD	ss4043289006	Apr 25, 2021 (155)
46	TOMMO_GENOMICS	ss5151878654	Apr 25, 2021 (155)
47	TOMMO_GENOMICS	ss5151878655	Apr 25, 2021 (155)
48	TOMMO_GENOMICS	ss5151878656	Apr 25, 2021 (155)
49	TOMMO_GENOMICS	ss5151878657	Apr 25, 2021 (155)
50	TOMMO_GENOMICS	ss5151878658	Apr 25, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5248453036	Oct 12, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5248453037	Oct 12, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5248453038	Oct 12, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5248453039	Oct 12, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5248453040	Oct 12, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5248453041	Oct 12, 2022 (156)
57	HUGCELL_USP	ss5448620465	Oct 12, 2022 (156)
58	HUGCELL_USP	ss5448620466	Oct 12, 2022 (156)
59	HUGCELL_USP	ss5448620467	Oct 12, 2022 (156)
60	HUGCELL_USP	ss5448620468	Oct 12, 2022 (156)
61	TOMMO_GENOMICS	ss5680650543	Oct 12, 2022 (156)
62	TOMMO_GENOMICS	ss5680650544	Oct 12, 2022 (156)
63	TOMMO_GENOMICS	ss5680650545	Oct 12, 2022 (156)
64	TOMMO_GENOMICS	ss5680650546	Oct 12, 2022 (156)
65	TOMMO_GENOMICS	ss5680650547	Oct 12, 2022 (156)
66	TOMMO_GENOMICS	ss5680650548	Oct 12, 2022 (156)
67	EVA	ss5820249987	Oct 12, 2022 (156)
68	EVA	ss5820249988	Oct 12, 2022 (156)
69	EVA	ss5852565436	Oct 12, 2022 (156)
70	1000Genomes	NC_000002.11 - 68523697	Oct 11, 2018 (152)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61509058 (NC_000002.12:68296564::TG 668/138976) Row 61509059 (NC_000002.12:68296564::TGTG 52505/138982) Row 61509061 (NC_000002.12:68296564::TGTGTG 586/139102)...	-	Apr 25, 2021 (155)
83	KOREAN population from KRGDB	NC_000002.11 - 68523697	Apr 25, 2020 (154)
84	8.3KJPN Submission ignored due to conflicting rows: Row 9847961 (NC_000002.11:68523696::TGTG 10257/16760) Row 9847962 (NC_000002.11:68523696::TGTGTG 328/16760) Row 9847963 (NC_000002.11:68523696::TG 67/16760)...	-	Apr 25, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 9847961 (NC_000002.11:68523696::TGTG 10257/16760) Row 9847962 (NC_000002.11:68523696::TGTGTG 328/16760) Row 9847963 (NC_000002.11:68523696::TG 67/16760)...	-	Apr 25, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 9847961 (NC_000002.11:68523696::TGTG 10257/16760) Row 9847962 (NC_000002.11:68523696::TGTGTG 328/16760) Row 9847963 (NC_000002.11:68523696::TG 67/16760)...	-	Apr 25, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 9847961 (NC_000002.11:68523696::TGTG 10257/16760) Row 9847962 (NC_000002.11:68523696::TGTGTG 328/16760) Row 9847963 (NC_000002.11:68523696::TG 67/16760)...	-	Apr 25, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 9847961 (NC_000002.11:68523696::TGTG 10257/16760) Row 9847962 (NC_000002.11:68523696::TGTGTG 328/16760) Row 9847963 (NC_000002.11:68523696::TG 67/16760)...	-	Apr 25, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 14487647 (NC_000002.12:68296564::TGTG 17279/28256) Row 14487648 (NC_000002.12:68296564::TGTGTG 556/28256) Row 14487649 (NC_000002.12:68296564::TGTGTGTGTG 124/28256)...	-	Oct 12, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 14487647 (NC_000002.12:68296564::TGTG 17279/28256) Row 14487648 (NC_000002.12:68296564::TGTGTG 556/28256) Row 14487649 (NC_000002.12:68296564::TGTGTGTGTG 124/28256)...	-	Oct 12, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 14487647 (NC_000002.12:68296564::TGTG 17279/28256) Row 14487648 (NC_000002.12:68296564::TGTGTG 556/28256) Row 14487649 (NC_000002.12:68296564::TGTGTGTGTG 124/28256)...	-	Oct 12, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 14487647 (NC_000002.12:68296564::TGTG 17279/28256) Row 14487648 (NC_000002.12:68296564::TGTGTG 556/28256) Row 14487649 (NC_000002.12:68296564::TGTGTGTGTG 124/28256)...	-	Oct 12, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 14487647 (NC_000002.12:68296564::TGTG 17279/28256) Row 14487648 (NC_000002.12:68296564::TGTGTG 556/28256) Row 14487649 (NC_000002.12:68296564::TGTGTGTGTG 124/28256)...	-	Oct 12, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 14487647 (NC_000002.12:68296564::TGTG 17279/28256) Row 14487648 (NC_000002.12:68296564::TGTGTG 556/28256) Row 14487649 (NC_000002.12:68296564::TGTGTGTGTG 124/28256)...	-	Oct 12, 2022 (156)
95	ALFA	NC_000002.12 - 68296565	Apr 25, 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
ss4043289006	NC_000002.12:68296564:TGTGTGTG:	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGT	(self)
ss4043289005	NC_000002.12:68296564:TGTG:	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	(self)
ss4043289004, ss5680650547	NC_000002.12:68296564:TG:	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss2989687235, ss5151878656	NC_000002.11:68523696::TG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss3063940644, ss4043288992, ss5248453038, ss5448620468, ss5680650546	NC_000002.12:68296564::TG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss326209777, ss326221726, ss326287134, ss551090392, ss551138127, ss552901267	NC_000002.10:68377200::TGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss288175703	NC_000002.10:68377217::GTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
8659033, 5112706, ss663322783, ss666151897, ss1368282687, ss1536292569, ss2624822607, ss2989687232, ss3783891359, ss3789473696, ss3794346639, ss3827036939, ss3897935312, ss5151878654, ss5820249987	NC_000002.11:68523696::TGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss3064791778, ss3647056987, ss3801265091, ss4043288993, ss5248453036, ss5448620465, ss5680650543, ss5852565436	NC_000002.12:68296564::TGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss95275760	NT_022184.15:47345600::GTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss2989687234, ss5151878655	NC_000002.11:68523696::TGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4043288995, ss5248453040, ss5680650544	NC_000002.12:68296564::TGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4043288996	NC_000002.12:68296564::TGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
8659033, ss1368282691, ss2989687233, ss5151878657, ss5820249988	NC_000002.11:68523696::TGTGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3065746023, ss3801265090, ss4043288997, ss5248453037, ss5448620467, ss5680650545	NC_000002.12:68296564::TGTGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss2989687231, ss3836928092, ss5151878658	NC_000002.11:68523696::TGTGTGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3842344053, ss4043288998, ss5248453039, ss5448620466, ss5680650548	NC_000002.12:68296564::TGTGTGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss2989687236	NC_000002.11:68523696::TGTGTGTGTGT… NC_000002.11:68523696::TGTGTGTGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4043288999, ss5248453041	NC_000002.12:68296564::TGTGTGTGTGT… NC_000002.12:68296564::TGTGTGTGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4043289000	NC_000002.12:68296564::TGTGTGTGTGT… NC_000002.12:68296564::TGTGTGTGTGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4043289001	NC_000002.12:68296564::TGTGTGTGTGT… NC_000002.12:68296564::TGTGTGTGTGTGTGTGTG	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
91322705	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000002.12:68296564:TGTGTGTGTGTG… NC_000002.12:68296564:TGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(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 rs140524601

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.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs140524601