Name: rs72671702
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.

rs72671702

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:66937149 (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: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.076765 (20319/264690, TOPMED)
T=0.075726 (10607/140070, GnomAD)
T=0.00209 (59/28258, 14KJPN) (+ 16 more)
T=0.06432 (1215/18890, ALFA)
T=0.00221 (37/16760, 8.3KJPN)
T=0.0759 (486/6404, 1000G_30x)
T=0.0713 (357/5008, 1000G)
T=0.0317 (142/4480, Estonian)
T=0.0545 (210/3854, ALSPAC)
T=0.0526 (195/3708, TWINSUK)
T=0.0044 (13/2922, KOREAN)
T=0.0027 (5/1832, Korea1K)
T=0.047 (47/998, GoNL)
T=0.037 (22/600, NorthernSweden)
T=0.106 (23/216, Qatari)
C=0.45 (26/58, SGDP_PRJ)
T=0.03 (1/40, GENOME_DK)
C=0.5 (4/8, Siberian)
T=0.5 (4/8, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MIER1 : 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	18890	C=0.93568	T=0.06432
European	Sub	14286	C=0.94841	T=0.05159
African	Sub	2946	C=0.8744	T=0.1256
African Others	Sub	114	C=0.877	T=0.123
African American	Sub	2832	C=0.8743	T=0.1257
Asian	Sub	112	C=1.000	T=0.000
East Asian	Sub	86	C=1.00	T=0.00
Other Asian	Sub	26	C=1.00	T=0.00
Latin American 1	Sub	146	C=0.870	T=0.130
Latin American 2	Sub	610	C=0.938	T=0.062
South Asian	Sub	98	C=0.95	T=0.05
Other	Sub	692	C=0.934	T=0.066

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
TopMed	Global	Study-wide	264690	C=0.923235	T=0.076765
gnomAD - Genomes	Global	Study-wide	140070	C=0.924274	T=0.075726
gnomAD - Genomes	European	Sub	75896	C=0.94568	T=0.05432
gnomAD - Genomes	African	Sub	41930	C=0.87207	T=0.12793
gnomAD - Genomes	American	Sub	13642	C=0.94121	T=0.05879
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.9570	T=0.0430
gnomAD - Genomes	East Asian	Sub	3134	C=0.9936	T=0.0064
gnomAD - Genomes	Other	Sub	2146	C=0.9278	T=0.0722
14KJPN	JAPANESE	Study-wide	28258	C=0.99791	T=0.00209
Allele Frequency Aggregator	Total	Global	18890	C=0.93568	T=0.06432
Allele Frequency Aggregator	European	Sub	14286	C=0.94841	T=0.05159
Allele Frequency Aggregator	African	Sub	2946	C=0.8744	T=0.1256
Allele Frequency Aggregator	Other	Sub	692	C=0.934	T=0.066
Allele Frequency Aggregator	Latin American 2	Sub	610	C=0.938	T=0.062
Allele Frequency Aggregator	Latin American 1	Sub	146	C=0.870	T=0.130
Allele Frequency Aggregator	Asian	Sub	112	C=1.000	T=0.000
Allele Frequency Aggregator	South Asian	Sub	98	C=0.95	T=0.05
8.3KJPN	JAPANESE	Study-wide	16760	C=0.99779	T=0.00221
1000Genomes_30x	Global	Study-wide	6404	C=0.9241	T=0.0759
1000Genomes_30x	African	Sub	1786	C=0.8533	T=0.1467
1000Genomes_30x	Europe	Sub	1266	C=0.9455	T=0.0545
1000Genomes_30x	South Asian	Sub	1202	C=0.9268	T=0.0732
1000Genomes_30x	East Asian	Sub	1170	C=0.9855	T=0.0145
1000Genomes_30x	American	Sub	980	C=0.949	T=0.051
1000Genomes	Global	Study-wide	5008	C=0.9287	T=0.0713
1000Genomes	African	Sub	1322	C=0.8578	T=0.1422
1000Genomes	East Asian	Sub	1008	C=0.9881	T=0.0119
1000Genomes	Europe	Sub	1006	C=0.9483	T=0.0517
1000Genomes	South Asian	Sub	978	C=0.930	T=0.070
1000Genomes	American	Sub	694	C=0.947	T=0.053
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.9683	T=0.0317
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.9455	T=0.0545
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.9474	T=0.0526
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.9956	T=0.0044
Korean Genome Project	KOREAN	Study-wide	1832	C=0.9973	T=0.0027
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.953	T=0.047
Northern Sweden	ACPOP	Study-wide	600	C=0.963	T=0.037
Qatari	Global	Study-wide	216	C=0.894	T=0.106
SGDP_PRJ	Global	Study-wide	58	C=0.45	T=0.55
The Danish reference pan genome	Danish	Study-wide	40	C=0.97	T=0.03
Siberian	Global	Study-wide	8	C=0.5	T=0.5

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 1	NC_000001.11:g.66937149C>T
GRCh37.p13 chr 1	NC_000001.10:g.67402832C>T
MIER1 RefSeqGene	NG_029847.1:g.17255C>T

Gene: MIER1, MIER1 transcriptional regulator (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MIER1 transcript variant 2	NM_001077700.3:c.169-2879… NM_001077700.3:c.169-2879C>T	N/A	Intron Variant
MIER1 transcript variant 3	NM_001077701.3:c.10-2879C… NM_001077701.3:c.10-2879C>T	N/A	Intron Variant
MIER1 transcript variant 4	NM_001077702.3:c.61-2879C… NM_001077702.3:c.61-2879C>T	N/A	Intron Variant
MIER1 transcript variant 5	NM_001077703.3:c.169-2879… NM_001077703.3:c.169-2879C>T	N/A	Intron Variant
MIER1 transcript variant 6	NM_001077704.3:c.10-2879C… NM_001077704.3:c.10-2879C>T	N/A	Intron Variant
MIER1 transcript variant 10	NM_001146110.2:c.61-2879C… NM_001146110.2:c.61-2879C>T	N/A	Intron Variant
MIER1 transcript variant 7	NM_001146111.2:c.61-2879C… NM_001146111.2:c.61-2879C>T	N/A	Intron Variant
MIER1 transcript variant 8	NM_001146112.2:c.-72-2879… NM_001146112.2:c.-72-2879C>T	N/A	Intron Variant
MIER1 transcript variant 9	NM_001146113.2:c.-34-2879… NM_001146113.2:c.-34-2879C>T	N/A	Intron Variant
MIER1 transcript variant 11	NM_001278215.2:c.61-2879C… NM_001278215.2:c.61-2879C>T	N/A	Intron Variant
MIER1 transcript variant 12	NM_001350530.2:c.243-2879… NM_001350530.2:c.243-2879C>T	N/A	Intron Variant
MIER1 transcript variant 1	NM_020948.4:c.61-2879C>T	N/A	Intron Variant
MIER1 transcript variant X1	XM_011541865.3:c.204-2879… XM_011541865.3:c.204-2879C>T	N/A	Intron Variant
MIER1 transcript variant X2	XM_017001919.2:c.81-2879C… XM_017001919.2:c.81-2879C>T	N/A	Intron Variant
MIER1 transcript variant X17	XM_017001920.2:c.81-2879C… XM_017001920.2:c.81-2879C>T	N/A	Intron Variant
MIER1 transcript variant X5	XM_017001923.2:c.243-2879… XM_017001923.2:c.243-2879C>T	N/A	Intron Variant
MIER1 transcript variant X6	XM_017001924.2:c.61-2879C… XM_017001924.2:c.61-2879C>T	N/A	Intron Variant
MIER1 transcript variant X9	XM_017001927.2:c.7-2879C>T	N/A	Intron Variant
MIER1 transcript variant X11	XM_017001928.3:c.7-2879C>T	N/A	Intron Variant
MIER1 transcript variant X10	XM_017001930.2:c.-31-2879… XM_017001930.2:c.-31-2879C>T	N/A	Intron Variant
MIER1 transcript variant X13	XM_017001931.2:c.-72-2879… XM_017001931.2:c.-72-2879C>T	N/A	Intron Variant
MIER1 transcript variant X14	XM_017001933.2:c.-34-2879… XM_017001933.2:c.-34-2879C>T	N/A	Intron Variant
MIER1 transcript variant X3	XM_047426255.1:c.72-2879C… XM_047426255.1:c.72-2879C>T	N/A	Intron Variant
MIER1 transcript variant X4	XM_047426256.1:c.72-2879C… XM_047426256.1:c.72-2879C>T	N/A	Intron Variant
MIER1 transcript variant X7	XM_047426260.1:c.61-2879C… XM_047426260.1:c.61-2879C>T	N/A	Intron Variant
MIER1 transcript variant X8	XM_047426263.1:c.61-2879C… XM_047426263.1:c.61-2879C>T	N/A	Intron Variant
MIER1 transcript variant X12	XM_047426264.1:c.-31-2879… XM_047426264.1:c.-31-2879C>T	N/A	Intron Variant
MIER1 transcript variant X15	XM_047426265.1:c.-34-2879… XM_047426265.1:c.-34-2879C>T	N/A	Intron Variant
MIER1 transcript variant X18	XM_047426266.1:c.243-2879… XM_047426266.1:c.243-2879C>T	N/A	Intron Variant
MIER1 transcript variant X16	XM_017001934.2:c.	N/A	Genic Upstream Transcript Variant
MIER1 transcript variant X19	XR_007062438.1:n.	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	C=	T
GRCh38.p14 chr 1	NC_000001.11:g.66937149=	NC_000001.11:g.66937149C>T
GRCh37.p13 chr 1	NC_000001.10:g.67402832=	NC_000001.10:g.67402832C>T
MIER1 RefSeqGene	NG_029847.1:g.17255=	NG_029847.1:g.17255C>T
MIER1 transcript variant 2	NM_001077700.2:c.169-2879=	NM_001077700.2:c.169-2879C>T
MIER1 transcript variant 2	NM_001077700.3:c.169-2879=	NM_001077700.3:c.169-2879C>T
MIER1 transcript variant 3	NM_001077701.2:c.10-2879=	NM_001077701.2:c.10-2879C>T
MIER1 transcript variant 3	NM_001077701.3:c.10-2879=	NM_001077701.3:c.10-2879C>T
MIER1 transcript variant 4	NM_001077702.2:c.61-2879=	NM_001077702.2:c.61-2879C>T
MIER1 transcript variant 4	NM_001077702.3:c.61-2879=	NM_001077702.3:c.61-2879C>T
MIER1 transcript variant 5	NM_001077703.2:c.169-2879=	NM_001077703.2:c.169-2879C>T
MIER1 transcript variant 5	NM_001077703.3:c.169-2879=	NM_001077703.3:c.169-2879C>T
MIER1 transcript variant 6	NM_001077704.2:c.10-2879=	NM_001077704.2:c.10-2879C>T
MIER1 transcript variant 6	NM_001077704.3:c.10-2879=	NM_001077704.3:c.10-2879C>T
MIER1 transcript variant 10	NM_001146110.1:c.61-2879=	NM_001146110.1:c.61-2879C>T
MIER1 transcript variant 10	NM_001146110.2:c.61-2879=	NM_001146110.2:c.61-2879C>T
MIER1 transcript variant 7	NM_001146111.1:c.61-2879=	NM_001146111.1:c.61-2879C>T
MIER1 transcript variant 7	NM_001146111.2:c.61-2879=	NM_001146111.2:c.61-2879C>T
MIER1 transcript variant 8	NM_001146112.1:c.-72-2879=	NM_001146112.1:c.-72-2879C>T
MIER1 transcript variant 8	NM_001146112.2:c.-72-2879=	NM_001146112.2:c.-72-2879C>T
MIER1 transcript variant 9	NM_001146113.1:c.-34-2879=	NM_001146113.1:c.-34-2879C>T
MIER1 transcript variant 9	NM_001146113.2:c.-34-2879=	NM_001146113.2:c.-34-2879C>T
MIER1 transcript variant 11	NM_001278215.1:c.61-2879=	NM_001278215.1:c.61-2879C>T
MIER1 transcript variant 11	NM_001278215.2:c.61-2879=	NM_001278215.2:c.61-2879C>T
MIER1 transcript variant 12	NM_001350530.2:c.243-2879=	NM_001350530.2:c.243-2879C>T
MIER1 transcript variant 1	NM_020948.3:c.61-2879=	NM_020948.3:c.61-2879C>T
MIER1 transcript variant 1	NM_020948.4:c.61-2879=	NM_020948.4:c.61-2879C>T
MIER1 transcript variant X1	XM_005271075.1:c.239-2874=	XM_005271075.1:c.239-2874C>T
MIER1 transcript variant X2	XM_005271076.1:c.61-2879=	XM_005271076.1:c.61-2879C>T
MIER1 transcript variant X3	XM_005271077.1:c.61-2879=	XM_005271077.1:c.61-2879C>T
MIER1 transcript variant X1	XM_011541865.3:c.204-2879=	XM_011541865.3:c.204-2879C>T
MIER1 transcript variant X2	XM_017001919.2:c.81-2879=	XM_017001919.2:c.81-2879C>T
MIER1 transcript variant X17	XM_017001920.2:c.81-2879=	XM_017001920.2:c.81-2879C>T
MIER1 transcript variant X5	XM_017001923.2:c.243-2879=	XM_017001923.2:c.243-2879C>T
MIER1 transcript variant X6	XM_017001924.2:c.61-2879=	XM_017001924.2:c.61-2879C>T
MIER1 transcript variant X9	XM_017001927.2:c.7-2879=	XM_017001927.2:c.7-2879C>T
MIER1 transcript variant X11	XM_017001928.3:c.7-2879=	XM_017001928.3:c.7-2879C>T
MIER1 transcript variant X10	XM_017001930.2:c.-31-2879=	XM_017001930.2:c.-31-2879C>T
MIER1 transcript variant X13	XM_017001931.2:c.-72-2879=	XM_017001931.2:c.-72-2879C>T
MIER1 transcript variant X14	XM_017001933.2:c.-34-2879=	XM_017001933.2:c.-34-2879C>T
MIER1 transcript variant X3	XM_047426255.1:c.72-2879=	XM_047426255.1:c.72-2879C>T
MIER1 transcript variant X4	XM_047426256.1:c.72-2879=	XM_047426256.1:c.72-2879C>T
MIER1 transcript variant X7	XM_047426260.1:c.61-2879=	XM_047426260.1:c.61-2879C>T
MIER1 transcript variant X8	XM_047426263.1:c.61-2879=	XM_047426263.1:c.61-2879C>T
MIER1 transcript variant X12	XM_047426264.1:c.-31-2879=	XM_047426264.1:c.-31-2879C>T
MIER1 transcript variant X15	XM_047426265.1:c.-34-2879=	XM_047426265.1:c.-34-2879C>T
MIER1 transcript variant X18	XM_047426266.1:c.243-2879=	XM_047426266.1:c.243-2879C>T

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#.

46 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss108274886	Feb 13, 2009 (130)
2	COMPLETE_GENOMICS	ss163473446	Jul 04, 2010 (132)
3	1000GENOMES	ss210545595	Jul 14, 2010 (132)
4	1000GENOMES	ss218431140	Jul 14, 2010 (132)
5	1000GENOMES	ss230568440	Jul 14, 2010 (132)
6	TISHKOFF	ss554207139	Apr 25, 2013 (138)
7	SSMP	ss648080775	Apr 25, 2013 (138)
8	EVA-GONL	ss975247340	Aug 21, 2014 (142)
9	JMKIDD_LAB	ss1067954120	Aug 21, 2014 (142)
10	1000GENOMES	ss1291223632	Aug 21, 2014 (142)
11	DDI	ss1425837547	Apr 01, 2015 (144)
12	EVA_GENOME_DK	ss1574120874	Apr 01, 2015 (144)
13	EVA_DECODE	ss1584616814	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1600350408	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1643344441	Apr 01, 2015 (144)
16	HAMMER_LAB	ss1794496405	Sep 08, 2015 (146)
17	WEILL_CORNELL_DGM	ss1918455375	Feb 12, 2016 (147)
18	JJLAB	ss2019745012	Sep 14, 2016 (149)
19	USC_VALOUEV	ss2147760805	Dec 20, 2016 (150)
20	HUMAN_LONGEVITY	ss2163194484	Dec 20, 2016 (150)
21	GNOMAD	ss2756081818	Nov 08, 2017 (151)
22	SWEGEN	ss2986949489	Nov 08, 2017 (151)
23	CSHL	ss3343493093	Nov 08, 2017 (151)
24	EGCUT_WGS	ss3655019519	Jul 12, 2019 (153)
25	EVA_DECODE	ss3686934675	Jul 12, 2019 (153)
26	ACPOP	ss3727119906	Jul 12, 2019 (153)
27	EVA	ss3746307116	Jul 12, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3799313825	Jul 12, 2019 (153)
29	EVA	ss3826214862	Apr 25, 2020 (154)
30	SGDP_PRJ	ss3849020619	Apr 25, 2020 (154)
31	KRGDB	ss3894048303	Apr 25, 2020 (154)
32	KOGIC	ss3944674370	Apr 25, 2020 (154)
33	TOPMED	ss4452656923	Apr 25, 2021 (155)
34	TOMMO_GENOMICS	ss5144321070	Apr 25, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5242556490	Oct 12, 2022 (156)
36	EVA	ss5319256589	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5443590988	Oct 12, 2022 (156)
38	EVA	ss5505880048	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5514977687	Oct 12, 2022 (156)
40	SANFORD_IMAGENETICS	ss5625693920	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5669199304	Oct 12, 2022 (156)
42	YY_MCH	ss5800668748	Oct 12, 2022 (156)
43	EVA	ss5832071259	Oct 12, 2022 (156)
44	EVA	ss5848941891	Oct 12, 2022 (156)
45	EVA	ss5908592618	Oct 12, 2022 (156)
46	EVA	ss5937532459	Oct 12, 2022 (156)
47	1000Genomes	NC_000001.10 - 67402832	Oct 11, 2018 (152)
48	1000Genomes_30x	NC_000001.11 - 66937149	Oct 12, 2022 (156)
49	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 67402832	Oct 11, 2018 (152)
50	Genetic variation in the Estonian population	NC_000001.10 - 67402832	Oct 11, 2018 (152)
51	The Danish reference pan genome	NC_000001.10 - 67402832	Apr 25, 2020 (154)
52	gnomAD - Genomes	NC_000001.11 - 66937149	Apr 25, 2021 (155)
53	Genome of the Netherlands Release 5	NC_000001.10 - 67402832	Apr 25, 2020 (154)
54	KOREAN population from KRGDB	NC_000001.10 - 67402832	Apr 25, 2020 (154)
55	Korean Genome Project	NC_000001.11 - 66937149	Apr 25, 2020 (154)
56	Northern Sweden	NC_000001.10 - 67402832	Jul 12, 2019 (153)
57	Qatari	NC_000001.10 - 67402832	Apr 25, 2020 (154)
58	SGDP_PRJ	NC_000001.10 - 67402832	Apr 25, 2020 (154)
59	Siberian	NC_000001.10 - 67402832	Apr 25, 2020 (154)
60	8.3KJPN	NC_000001.10 - 67402832	Apr 25, 2021 (155)
61	14KJPN	NC_000001.11 - 66937149	Oct 12, 2022 (156)
62	TopMed	NC_000001.11 - 66937149	Apr 25, 2021 (155)
63	UK 10K study - Twins	NC_000001.10 - 67402832	Oct 11, 2018 (152)
64	ALFA	NC_000001.11 - 66937149	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
ss108274886, ss163473446, ss210545595, ss1584616814	NC_000001.9:67175419:C:T	NC_000001.11:66937148:C:T	(self)
1953800, 1070294, 757767, 1536367, 456810, 1225697, 404771, 497305, 1037599, 277159, 2290377, 1070294, ss218431140, ss230568440, ss554207139, ss648080775, ss975247340, ss1067954120, ss1291223632, ss1425837547, ss1574120874, ss1600350408, ss1643344441, ss1794496405, ss1918455375, ss2019745012, ss2147760805, ss2756081818, ss2986949489, ss3343493093, ss3655019519, ss3727119906, ss3746307116, ss3826214862, ss3849020619, ss3894048303, ss5144321070, ss5319256589, ss5505880048, ss5625693920, ss5832071259, ss5937532459	NC_000001.10:67402831:C:T	NC_000001.11:66937148:C:T	(self)
2503622, 13778727, 1052371, 3036408, 16263258, 5729902726, ss2163194484, ss3686934675, ss3799313825, ss3944674370, ss4452656923, ss5242556490, ss5443590988, ss5514977687, ss5669199304, ss5800668748, ss5848941891, ss5908592618	NC_000001.11:66937148:C:T	NC_000001.11:66937148:C:T	(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 rs72671702

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

rs72671702