Name: rs3070655
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.

rs3070655

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:15658755-15658769 (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(A)₅ / delAA / delA / dupA / du…
del(A)₅ / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.2646 (1971/7450, ALFA)
(A)₁₅=0.3395 (1700/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DDI2 : Intron Variant
RSC1A1 : 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	7450	AAAAAAAAAAAAAAA=0.5515	AAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0004, AAAAAAAAAAAAAAAA=0.2646, AAAAAAAAAAAAAAAAA=0.1835, AAAAAAAAAAAAAAAAAA=0.0000	0.646697	0.185868	0.167435	32
European	Sub	7186	AAAAAAAAAAAAAAA=0.5359	AAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0004, AAAAAAAAAAAAAAAA=0.2736, AAAAAAAAAAAAAAAAA=0.1901, AAAAAAAAAAAAAAAAAA=0.0000	0.628791	0.194905	0.176304	32
African	Sub	84	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	6	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	78	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	6	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	12	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	86	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	22	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	54	AAAAAAAAAAAAAAA=0.89	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.09, AAAAAAAAAAAAAAAAA=0.02, AAAAAAAAAAAAAAAAAA=0.00	0.923077	0.076923	0.0	14

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	7450	(A)₁₅=0.5515	del(A)₅=0.0000, delAA=0.0000, delA=0.0004, dupA=0.2646, dupAA=0.1835, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	7186	(A)₁₅=0.5359	del(A)₅=0.0000, delAA=0.0000, delA=0.0004, dupA=0.2736, dupAA=0.1901, dupAAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	86	(A)₁₅=1.00	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	African	Sub	84	(A)₁₅=1.00	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Other	Sub	54	(A)₁₅=0.89	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.09, dupAA=0.02, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(A)₁₅=1.00	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(A)₁₅=1.00	del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	6	(A)₁₅=1.0	del(A)₅=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.6605
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.7799
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.7421
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.5726
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.555
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.591

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.15658765_15658769del
GRCh38.p14 chr 1	NC_000001.11:g.15658768_15658769del
GRCh38.p14 chr 1	NC_000001.11:g.15658769del
GRCh38.p14 chr 1	NC_000001.11:g.15658769dup
GRCh38.p14 chr 1	NC_000001.11:g.15658768_15658769dup
GRCh38.p14 chr 1	NC_000001.11:g.15658767_15658769dup
GRCh37.p13 chr 1	NC_000001.10:g.15985260_15985264del
GRCh37.p13 chr 1	NC_000001.10:g.15985263_15985264del
GRCh37.p13 chr 1	NC_000001.10:g.15985264del
GRCh37.p13 chr 1	NC_000001.10:g.15985264dup
GRCh37.p13 chr 1	NC_000001.10:g.15985263_15985264dup
GRCh37.p13 chr 1	NC_000001.10:g.15985262_15985264dup

Gene: DDI2, DNA damage inducible 1 homolog 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DDI2 transcript	NM_032341.5:c.47-1072_4… NM_032341.5:c.47-1072_47-1068del	N/A	Intron Variant

Gene: RSC1A1, regulator of solute carriers 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
RSC1A1 transcript	NM_006511.3:c.	N/A	Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(A)₁₅=	del(A)₅	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 1	NC_000001.11:g.15658755_15658769=	NC_000001.11:g.15658765_15658769del	NC_000001.11:g.15658768_15658769del	NC_000001.11:g.15658769del	NC_000001.11:g.15658769dup	NC_000001.11:g.15658768_15658769dup	NC_000001.11:g.15658767_15658769dup
GRCh37.p13 chr 1	NC_000001.10:g.15985250_15985264=	NC_000001.10:g.15985260_15985264del	NC_000001.10:g.15985263_15985264del	NC_000001.10:g.15985264del	NC_000001.10:g.15985264dup	NC_000001.10:g.15985263_15985264dup	NC_000001.10:g.15985262_15985264dup
DDI2 transcript	NM_032341.4:c.*47-1082=	NM_032341.4:c.47-1072_47-1068del	NM_032341.4:c.47-1069_47-1068del	NM_032341.4:c.*47-1068del	NM_032341.4:c.*47-1068dup	NM_032341.4:c.47-1069_47-1068dup	NM_032341.4:c.47-1070_47-1068dup
DDI2 transcript	NM_032341.5:c.*47-1082=	NM_032341.5:c.47-1072_47-1068del	NM_032341.5:c.47-1069_47-1068del	NM_032341.5:c.*47-1068del	NM_032341.5:c.*47-1068dup	NM_032341.5:c.47-1069_47-1068dup	NM_032341.5:c.47-1070_47-1068dup
DDI2 transcript variant X1	XM_005246017.1:c.1184-1082=	XM_005246017.1:c.1184-1072_1184-1068del	XM_005246017.1:c.1184-1069_1184-1068del	XM_005246017.1:c.1184-1068del	XM_005246017.1:c.1184-1068dup	XM_005246017.1:c.1184-1069_1184-1068dup	XM_005246017.1:c.1184-1070_1184-1068dup
DDI2 transcript variant X2	XM_005246018.1:c.-32-1082=	XM_005246018.1:c.-32-1072_-32-1068del	XM_005246018.1:c.-32-1069_-32-1068del	XM_005246018.1:c.-32-1068del	XM_005246018.1:c.-32-1068dup	XM_005246018.1:c.-32-1069_-32-1068dup	XM_005246018.1:c.-32-1070_-32-1068dup

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#.

47 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4302032	Jan 05, 2002 (102)
2	ABI	ss41230063	Mar 13, 2006 (126)
3	HGSV	ss82571556	Dec 16, 2007 (130)
4	GMI	ss287952516	Sep 14, 2016 (149)
5	PJP	ss294567063	May 09, 2011 (137)
6	1000GENOMES	ss1367663978	Aug 21, 2014 (142)
7	EVA_UK10K_TWINSUK	ss1700298346	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1700298348	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1700298350	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1700298352	Apr 01, 2015 (144)
11	SYSTEMSBIOZJU	ss2624295888	Nov 08, 2017 (151)
12	SWEGEN	ss2986359474	Nov 08, 2017 (151)
13	MCHAISSO	ss3064391060	Nov 08, 2017 (151)
14	URBANLAB	ss3646607628	Oct 11, 2018 (152)
15	EVA_DECODE	ss3686229231	Jul 12, 2019 (153)
16	EVA_DECODE	ss3686229232	Jul 12, 2019 (153)
17	EVA_DECODE	ss3686229233	Jul 12, 2019 (153)
18	ACPOP	ss3726819751	Jul 12, 2019 (153)
19	ACPOP	ss3726819752	Jul 12, 2019 (153)
20	PACBIO	ss3783333210	Jul 12, 2019 (153)
21	PACBIO	ss3789006185	Jul 12, 2019 (153)
22	PACBIO	ss3793878906	Jul 12, 2019 (153)
23	KHV_HUMAN_GENOMES	ss3798890696	Jul 12, 2019 (153)
24	EVA	ss3826039785	Apr 25, 2020 (154)
25	EVA	ss3836407405	Apr 25, 2020 (154)
26	EVA	ss3841811612	Apr 25, 2020 (154)
27	KOGIC	ss3943899205	Apr 25, 2020 (154)
28	KOGIC	ss3943899206	Apr 25, 2020 (154)
29	GNOMAD	ss3988886731	Apr 25, 2021 (155)
30	GNOMAD	ss3988886732	Apr 25, 2021 (155)
31	GNOMAD	ss3988886733	Apr 25, 2021 (155)
32	GNOMAD	ss3988886734	Apr 25, 2021 (155)
33	GNOMAD	ss3988886735	Apr 25, 2021 (155)
34	TOMMO_GENOMICS	ss5142640010	Apr 25, 2021 (155)
35	TOMMO_GENOMICS	ss5142640011	Apr 25, 2021 (155)
36	TOMMO_GENOMICS	ss5142640012	Apr 25, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5241301866	Oct 17, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5241301867	Oct 17, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5241301868	Oct 17, 2022 (156)
40	HUGCELL_USP	ss5442481789	Oct 17, 2022 (156)
41	HUGCELL_USP	ss5442481790	Oct 17, 2022 (156)
42	TOMMO_GENOMICS	ss5666997964	Oct 17, 2022 (156)
43	TOMMO_GENOMICS	ss5666997965	Oct 17, 2022 (156)
44	TOMMO_GENOMICS	ss5666997966	Oct 17, 2022 (156)
45	EVA	ss5831584945	Oct 17, 2022 (156)
46	EVA	ss5831584946	Oct 17, 2022 (156)
47	EVA	ss5907170861	Oct 17, 2022 (156)
48	1000Genomes	NC_000001.10 - 15985250	Oct 11, 2018 (152)
49	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 256978 (NC_000001.10:15985249::A 1594/3854) Row 256979 (NC_000001.10:15985249::AA 1115/3854)	-	Oct 11, 2018 (152)
50	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 256978 (NC_000001.10:15985249::A 1594/3854) Row 256979 (NC_000001.10:15985249::AA 1115/3854)	-	Oct 11, 2018 (152)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3418518 (NC_000001.11:15658754::A 59533/133970) Row 3418519 (NC_000001.11:15658754::AA 45567/133876) Row 3418520 (NC_000001.11:15658754::AAA 76/134084)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3418518 (NC_000001.11:15658754::A 59533/133970) Row 3418519 (NC_000001.11:15658754::AA 45567/133876) Row 3418520 (NC_000001.11:15658754::AAA 76/134084)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3418518 (NC_000001.11:15658754::A 59533/133970) Row 3418519 (NC_000001.11:15658754::AA 45567/133876) Row 3418520 (NC_000001.11:15658754::AAA 76/134084)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3418518 (NC_000001.11:15658754::A 59533/133970) Row 3418519 (NC_000001.11:15658754::AA 45567/133876) Row 3418520 (NC_000001.11:15658754::AAA 76/134084)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3418518 (NC_000001.11:15658754::A 59533/133970) Row 3418519 (NC_000001.11:15658754::AA 45567/133876) Row 3418520 (NC_000001.11:15658754::AAA 76/134084)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3418518 (NC_000001.11:15658754::A 59533/133970) Row 3418519 (NC_000001.11:15658754::AA 45567/133876) Row 3418520 (NC_000001.11:15658754::AAA 76/134084)...	-	Apr 25, 2021 (155)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 277206 (NC_000001.11:15658754::A 1357/1832) Row 277207 (NC_000001.11:15658754::AA 182/1832)	-	Apr 25, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 277206 (NC_000001.11:15658754::A 1357/1832) Row 277207 (NC_000001.11:15658754::AA 182/1832)	-	Apr 25, 2020 (154)
59	Northern Sweden Submission ignored due to conflicting rows: Row 104616 (NC_000001.10:15985249::AA 155/594) Row 104617 (NC_000001.10:15985249::A 299/594)	-	Jul 12, 2019 (153)
60	Northern Sweden Submission ignored due to conflicting rows: Row 104616 (NC_000001.10:15985249::AA 155/594) Row 104617 (NC_000001.10:15985249::A 299/594)	-	Jul 12, 2019 (153)
61	8.3KJPN Submission ignored due to conflicting rows: Row 609317 (NC_000001.10:15985249::A 13626/16758) Row 609318 (NC_000001.10:15985249::AA 1168/16758) Row 609319 (NC_000001.10:15985249:A: 7/16758)	-	Apr 25, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 609317 (NC_000001.10:15985249::A 13626/16758) Row 609318 (NC_000001.10:15985249::AA 1168/16758) Row 609319 (NC_000001.10:15985249:A: 7/16758)	-	Apr 25, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 609317 (NC_000001.10:15985249::A 13626/16758) Row 609318 (NC_000001.10:15985249::AA 1168/16758) Row 609319 (NC_000001.10:15985249:A: 7/16758)	-	Apr 25, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 835068 (NC_000001.11:15658754::A 22882/28258) Row 835069 (NC_000001.11:15658754::AA 2015/28258) Row 835070 (NC_000001.11:15658754:A: 5/28258)	-	Oct 17, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 835068 (NC_000001.11:15658754::A 22882/28258) Row 835069 (NC_000001.11:15658754::AA 2015/28258) Row 835070 (NC_000001.11:15658754:A: 5/28258)	-	Oct 17, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 835068 (NC_000001.11:15658754::A 22882/28258) Row 835069 (NC_000001.11:15658754::AA 2015/28258) Row 835070 (NC_000001.11:15658754:A: 5/28258)	-	Oct 17, 2022 (156)
67	UK 10K study - Twins Submission ignored due to conflicting rows: Row 256978 (NC_000001.10:15985249::A 1490/3708) Row 256979 (NC_000001.10:15985249::AA 1055/3708)	-	Oct 11, 2018 (152)
68	UK 10K study - Twins Submission ignored due to conflicting rows: Row 256978 (NC_000001.10:15985249::A 1490/3708) Row 256979 (NC_000001.10:15985249::AA 1055/3708)	-	Oct 11, 2018 (152)
69	ALFA	NC_000001.11 - 15658755	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).

Associated ID	History Updated (Build)
rs61342754	May 23, 2008 (130)
rs386353825	Aug 21, 2014 (142)
rs35355637	May 11, 2012 (137)
rs71641596	May 11, 2012 (137)
rs146123000	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3988886735	NC_000001.11:15658754:AAAAA:	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
3873604508	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss3988886734	NC_000001.11:15658754:AA:	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
3873604508	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss2986359474, ss5142640012	NC_000001.10:15985249:A:	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3686229233, ss5666997966	NC_000001.11:15658754:A:	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
3873604508	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss294567063	NC_000001.9:15857837::A	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss287952516	NC_000001.9:15857851::A	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
489988, ss1367663978, ss1700298346, ss1700298348, ss2624295888, ss3726819752, ss3783333210, ss3789006185, ss3793878906, ss3826039785, ss3836407405, ss5142640010, ss5831584945	NC_000001.10:15985249::A	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3646607628, ss3798890696, ss3841811612, ss3943899205, ss3988886731, ss5241301867, ss5442481789, ss5666997964, ss5907170861	NC_000001.11:15658754::A	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
3873604508	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3686229232	NC_000001.11:15658755::A	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss41230063	NT_004610.19:2665337::A	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss82571556	NT_004610.19:2665352::A	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss287952516	NC_000001.9:15857851::AA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1700298350, ss1700298352, ss3726819751, ss5142640011, ss5831584946	NC_000001.10:15985249::AA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3064391060, ss3943899206, ss3988886732, ss5241301866, ss5442481790, ss5666997965	NC_000001.11:15658754::AA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
3873604508	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3686229231	NC_000001.11:15658755::AA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4302032	NT_004610.19:2665352::AA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3988886733, ss5241301868	NC_000001.11:15658754::AAA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
3873604508	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:15658754:AAAAAAAAAAAA… NC_000001.11:15658754:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(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 rs3070655

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

rs3070655