Name: rs71832912
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.

rs71832912

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:4313626-4313644 (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: delCTCT / delCT / dupCT / dupCTCT …
delCTCT / delCT / dupCT / dupCTCT / dup(CT)₃ / dup(CT)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupCT=0.00213 (38/17880, ALFA)
dupCT=0.0224 (112/5008, 1000G)
dupCT=0.022 (13/600, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UBE2G1 : 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	HTRZ	HWEP
Total	Global	17880	TCTCTCTCTCTCTCTCTCT=0.99771	TCTCTCTCTCTCTCT=0.00000, TCTCTCTCTCTCTCTCT=0.00000, TCTCTCTCTCTCTCTCTCTCT=0.00213, TCTCTCTCTCTCTCTCTCTCTCT=0.00017, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00000	0.995748	0.004252	0
European	Sub	13972	TCTCTCTCTCTCTCTCTCT=0.99707	TCTCTCTCTCTCTCT=0.00000, TCTCTCTCTCTCTCTCT=0.00000, TCTCTCTCTCTCTCTCTCTCT=0.00272, TCTCTCTCTCTCTCTCTCTCTCT=0.00021, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00000	0.994558	0.005442	0
African	Sub	2488	TCTCTCTCTCTCTCTCTCT=1.0000	TCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	1.0	0.0	N/A
African Others	Sub	102	TCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	N/A
African American	Sub	2386	TCTCTCTCTCTCTCTCTCT=1.0000	TCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	1.0	0.0	N/A
Asian	Sub	112	TCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	N/A
East Asian	Sub	86	TCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	N/A
Other Asian	Sub	26	TCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	N/A
Latin American 1	Sub	138	TCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	N/A
Latin American 2	Sub	602	TCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	N/A
South Asian	Sub	98	TCTCTCTCTCTCTCTCTCT=1.00	TCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCT=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	N/A
Other	Sub	470	TCTCTCTCTCTCTCTCTCT=1.000	TCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCT=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	N/A

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
Allele Frequency Aggregator	Total	Global	17880	(TC)₉T=0.99771	delCTCT=0.00000, delCT=0.00000, dupCT=0.00213, dupCTCT=0.00017, dup(CT)₃=0.00000, dup(CT)₄=0.00000
Allele Frequency Aggregator	European	Sub	13972	(TC)₉T=0.99707	delCTCT=0.00000, delCT=0.00000, dupCT=0.00272, dupCTCT=0.00021, dup(CT)₃=0.00000, dup(CT)₄=0.00000
Allele Frequency Aggregator	African	Sub	2488	(TC)₉T=1.0000	delCTCT=0.0000, delCT=0.0000, dupCT=0.0000, dupCTCT=0.0000, dup(CT)₃=0.0000, dup(CT)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	602	(TC)₉T=1.000	delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000
Allele Frequency Aggregator	Other	Sub	470	(TC)₉T=1.000	delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	(TC)₉T=1.000	delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000
Allele Frequency Aggregator	Asian	Sub	112	(TC)₉T=1.000	delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(TC)₉T=1.00	delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupCT=0.0224
1000Genomes	African	Sub	1322	- No frequency provided	dupCT=0.0756
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupCT=0.0030
1000Genomes	Europe	Sub	1006	- No frequency provided	dupCT=0.0040
1000Genomes	South Asian	Sub	978	- No frequency provided	dupCT=0.001
1000Genomes	American	Sub	694	- No frequency provided	dupCT=0.006
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupCT=0.022

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 17	NC_000017.11:g.4313627CT[7]
GRCh38.p14 chr 17	NC_000017.11:g.4313627CT[8]
GRCh38.p14 chr 17	NC_000017.11:g.4313627CT[10]
GRCh38.p14 chr 17	NC_000017.11:g.4313627CT[11]
GRCh38.p14 chr 17	NC_000017.11:g.4313627CT[12]
GRCh38.p14 chr 17	NC_000017.11:g.4313627CT[13]
GRCh37.p13 chr 17	NC_000017.10:g.4216922CT[7]
GRCh37.p13 chr 17	NC_000017.10:g.4216922CT[8]
GRCh37.p13 chr 17	NC_000017.10:g.4216922CT[10]
GRCh37.p13 chr 17	NC_000017.10:g.4216922CT[11]
GRCh37.p13 chr 17	NC_000017.10:g.4216922CT[12]
GRCh37.p13 chr 17	NC_000017.10:g.4216922CT[13]

Gene: UBE2G1, ubiquitin conjugating enzyme E2 G1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UBE2G1 transcript	NM_003342.5:c.47-6520GA[7]	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	(TC)₉T=	delCTCT	delCT	dupCT	dupCTCT	dup(CT)₃	dup(CT)₄
GRCh38.p14 chr 17	NC_000017.11:g.4313626_4313644=	NC_000017.11:g.4313627CT[7]	NC_000017.11:g.4313627CT[8]	NC_000017.11:g.4313627CT[10]	NC_000017.11:g.4313627CT[11]	NC_000017.11:g.4313627CT[12]	NC_000017.11:g.4313627CT[13]
GRCh37.p13 chr 17	NC_000017.10:g.4216921_4216939=	NC_000017.10:g.4216922CT[7]	NC_000017.10:g.4216922CT[8]	NC_000017.10:g.4216922CT[10]	NC_000017.10:g.4216922CT[11]	NC_000017.10:g.4216922CT[12]	NC_000017.10:g.4216922CT[13]
UBE2G1 transcript	NM_003342.4:c.47-6503=	NM_003342.4:c.47-6520GA[7]	NM_003342.4:c.47-6520GA[8]	NM_003342.4:c.47-6520GA[10]	NM_003342.4:c.47-6520GA[11]	NM_003342.4:c.47-6520GA[12]	NM_003342.4:c.47-6520GA[13]
UBE2G1 transcript	NM_003342.5:c.47-6503=	NM_003342.5:c.47-6520GA[7]	NM_003342.5:c.47-6520GA[8]	NM_003342.5:c.47-6520GA[10]	NM_003342.5:c.47-6520GA[11]	NM_003342.5:c.47-6520GA[12]	NM_003342.5:c.47-6520GA[13]

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#.

48 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss327887615	Jan 10, 2018 (151)
2	1000GENOMES	ss328209246	Jan 10, 2018 (151)
3	LUNTER	ss552504417	Jan 10, 2018 (151)
4	LUNTER	ss552847725	Jan 10, 2018 (151)
5	TISHKOFF	ss564651988	Apr 25, 2013 (138)
6	SSMP	ss664358086	Apr 01, 2015 (144)
7	1000GENOMES	ss1376312706	Aug 21, 2014 (142)
8	EVA_UK10K_ALSPAC	ss1708665465	Jan 10, 2018 (151)
9	EVA_UK10K_TWINSUK	ss1708665517	Jan 10, 2018 (151)
10	EVA_UK10K_TWINSUK	ss1710717800	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710717802	Apr 01, 2015 (144)
12	HAMMER_LAB	ss1808679741	Sep 08, 2015 (146)
13	SWEGEN	ss3015111168	Nov 08, 2017 (151)
14	EVA_DECODE	ss3699983289	Jul 13, 2019 (153)
15	EVA_DECODE	ss3699983290	Jul 13, 2019 (153)
16	EVA_DECODE	ss3699983291	Jul 13, 2019 (153)
17	ACPOP	ss3741827556	Jul 13, 2019 (153)
18	PACBIO	ss3788135180	Jul 13, 2019 (153)
19	PACBIO	ss3793105562	Jul 13, 2019 (153)
20	PACBIO	ss3797991135	Jul 13, 2019 (153)
21	KHV_HUMAN_GENOMES	ss3819658302	Jul 13, 2019 (153)
22	KHV_HUMAN_GENOMES	ss3819658303	Jul 13, 2019 (153)
23	KHV_HUMAN_GENOMES	ss3819658304	Jul 13, 2019 (153)
24	GNOMAD	ss4307120149	Apr 26, 2021 (155)
25	GNOMAD	ss4307120150	Apr 26, 2021 (155)
26	GNOMAD	ss4307120151	Apr 26, 2021 (155)
27	GNOMAD	ss4307120152	Apr 26, 2021 (155)
28	GNOMAD	ss4307120153	Apr 26, 2021 (155)
29	GNOMAD	ss4307120154	Apr 26, 2021 (155)
30	TOPMED	ss5027801997	Apr 26, 2021 (155)
31	TOPMED	ss5027801998	Apr 26, 2021 (155)
32	TOPMED	ss5027801999	Apr 26, 2021 (155)
33	TOPMED	ss5027802000	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5221262144	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5221262145	Apr 26, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5302248955	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5302248956	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5302248957	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5302248958	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5495442934	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5495442935	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5495442936	Oct 16, 2022 (156)
43	EVA	ss5511712114	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5776785831	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5776785832	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5776785833	Oct 16, 2022 (156)
47	EVA	ss5833650872	Oct 16, 2022 (156)
48	EVA	ss5833650873	Oct 16, 2022 (156)
49	1000Genomes	NC_000017.10 - 4216921	Oct 12, 2018 (152)
50	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39330516 (NC_000017.10:4216920:TC: 397/3854) Row 39330517 (NC_000017.10:4216920::TC 56/3854)	-	Oct 12, 2018 (152)
51	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39330516 (NC_000017.10:4216920:TC: 397/3854) Row 39330517 (NC_000017.10:4216920::TC 56/3854)	-	Oct 12, 2018 (152)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500069193 (NC_000017.11:4313625::TC 3655/137978) Row 500069194 (NC_000017.11:4313625::TCTC 35/138010) Row 500069195 (NC_000017.11:4313625::TCTCTC 1/138010)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500069193 (NC_000017.11:4313625::TC 3655/137978) Row 500069194 (NC_000017.11:4313625::TCTC 35/138010) Row 500069195 (NC_000017.11:4313625::TCTCTC 1/138010)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500069193 (NC_000017.11:4313625::TC 3655/137978) Row 500069194 (NC_000017.11:4313625::TCTC 35/138010) Row 500069195 (NC_000017.11:4313625::TCTCTC 1/138010)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500069193 (NC_000017.11:4313625::TC 3655/137978) Row 500069194 (NC_000017.11:4313625::TCTC 35/138010) Row 500069195 (NC_000017.11:4313625::TCTCTC 1/138010)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500069193 (NC_000017.11:4313625::TC 3655/137978) Row 500069194 (NC_000017.11:4313625::TCTC 35/138010) Row 500069195 (NC_000017.11:4313625::TCTCTC 1/138010)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500069193 (NC_000017.11:4313625::TC 3655/137978) Row 500069194 (NC_000017.11:4313625::TCTC 35/138010) Row 500069195 (NC_000017.11:4313625::TCTCTC 1/138010)...	-	Apr 26, 2021 (155)
58	Northern Sweden	NC_000017.10 - 4216921	Jul 13, 2019 (153)
59	8.3KJPN Submission ignored due to conflicting rows: Row 79231451 (NC_000017.10:4216920:TC: 8/16760) Row 79231452 (NC_000017.10:4216920::TC 19/16760)	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 79231451 (NC_000017.10:4216920:TC: 8/16760) Row 79231452 (NC_000017.10:4216920::TC 19/16760)	-	Apr 26, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 110622935 (NC_000017.11:4313625::TC 36/28258) Row 110622936 (NC_000017.11:4313625:TC: 5/28258) Row 110622937 (NC_000017.11:4313625:TCTC: 1/28258)	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 110622935 (NC_000017.11:4313625::TC 36/28258) Row 110622936 (NC_000017.11:4313625:TC: 5/28258) Row 110622937 (NC_000017.11:4313625:TCTC: 1/28258)	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 110622935 (NC_000017.11:4313625::TC 36/28258) Row 110622936 (NC_000017.11:4313625:TC: 5/28258) Row 110622937 (NC_000017.11:4313625:TCTC: 1/28258)	-	Oct 16, 2022 (156)
64	TopMed Submission ignored due to conflicting rows: Row 243347659 (NC_000017.11:4313625::TC 7128/264690) Row 243347660 (NC_000017.11:4313625::TCTC 59/264690) Row 243347661 (NC_000017.11:4313625::TCTCTC 1/264690)...	-	Apr 26, 2021 (155)
65	TopMed Submission ignored due to conflicting rows: Row 243347659 (NC_000017.11:4313625::TC 7128/264690) Row 243347660 (NC_000017.11:4313625::TCTC 59/264690) Row 243347661 (NC_000017.11:4313625::TCTCTC 1/264690)...	-	Apr 26, 2021 (155)
66	TopMed Submission ignored due to conflicting rows: Row 243347659 (NC_000017.11:4313625::TC 7128/264690) Row 243347660 (NC_000017.11:4313625::TCTC 59/264690) Row 243347661 (NC_000017.11:4313625::TCTCTC 1/264690)...	-	Apr 26, 2021 (155)
67	TopMed Submission ignored due to conflicting rows: Row 243347659 (NC_000017.11:4313625::TC 7128/264690) Row 243347660 (NC_000017.11:4313625::TCTC 59/264690) Row 243347661 (NC_000017.11:4313625::TCTCTC 1/264690)...	-	Apr 26, 2021 (155)
68	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39330516 (NC_000017.10:4216920:TC: 380/3708) Row 39330517 (NC_000017.10:4216920::TC 55/3708)	-	Oct 12, 2018 (152)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39330516 (NC_000017.10:4216920:TC: 380/3708) Row 39330517 (NC_000017.10:4216920::TC 55/3708)	-	Oct 12, 2018 (152)
70	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 8713458 (NC_000017.10:4216920:TCTC: 1/211) Row 8713459 (NC_000017.10:4216920::TC 1/211)	-	Jul 13, 2019 (153)
71	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 8713458 (NC_000017.10:4216920:TCTC: 1/211) Row 8713459 (NC_000017.10:4216920::TC 1/211)	-	Jul 13, 2019 (153)
72	ALFA	NC_000017.11 - 4313626	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)
rs149598001	May 11, 2012 (137)
rs368335968	May 15, 2013 (138)
rs371608871	May 13, 2013 (138)
rs796507619	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
	NC_000017.10:4216920:TCTC:	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCT	(self)
ss3699983289, ss3819658302, ss4307120154, ss5027802000, ss5302248955, ss5495442935, ss5776785833	NC_000017.11:4313625:TCTC:	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCT	(self)
374690259	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCT	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCT	(self)
ss327887615, ss328209246, ss552504417, ss552847725	NC_000017.9:4163669:TC:	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
ss1708665465, ss1708665517, ss5221262144, ss5511712114, ss5833650872	NC_000017.10:4216920:TC:	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
ss4307120153, ss5302248957, ss5495442934, ss5776785832	NC_000017.11:4313625:TC:	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
374690259	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
ss3699983290	NC_000017.11:4313627:TC:	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT	(self)
70915632, 15112421, ss664358086, ss1376312706, ss1808679741, ss3015111168, ss3741827556, ss3788135180, ss3793105562, ss3797991135, ss5221262145, ss5833650873	NC_000017.10:4216920::TC	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
ss1710717800, ss1710717802	NC_000017.10:4216922::TC	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
ss564651988	NC_000017.10:4216939::CT	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
ss3819658303, ss4307120149, ss5027801997, ss5302248956, ss5495442936, ss5776785831	NC_000017.11:4313625::TC	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
374690259	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
ss3699983291, ss3819658304	NC_000017.11:4313629::TC	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT	(self)
ss4307120150, ss5027801998, ss5302248958	NC_000017.11:4313625::TCTC	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
374690259	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4307120151, ss5027801999	NC_000017.11:4313625::TCTCTC	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
374690259	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4307120152	NC_000017.11:4313625::TCTCTCTC	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
374690259	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2379950559	NC_000017.10:4216920::TCTCTC	NC_000017.11:4313625:TCTCTCTCTCTCT… NC_000017.11:4313625:TCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs71832912

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71832912