Name: rs60893428
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.

rs60893428

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:9634256-9634269 (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)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.287755 (76166/264690, TOPMED)
delAA=0.1786 (1785/9996, ALFA)
delAA=0.3025 (1515/5008, 1000G) (+ 1 more)
delAA=0.35 (14/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PER3P1 : 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	9996	AAAAAAAAAAAAAA=0.8082	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.1786, AAAAAAAAAAAAA=0.0132, AAAAAAAAAAAAAAA=0.0000	0.717954	0.076417	0.205629	32
European	Sub	7726	AAAAAAAAAAAAAA=0.7523	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.2308, AAAAAAAAAAAAA=0.0170, AAAAAAAAAAAAAAA=0.0000	0.632833	0.099625	0.267542	32
African	Sub	1624	AAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	70	AAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1554	AAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	38	AAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	36	AAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	74	AAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	252	AAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	42	AAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	240	AAAAAAAAAAAAAA=0.988	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.008, AAAAAAAAAAAAA=0.004, AAAAAAAAAAAAAAA=0.000	0.983193	0.0	0.016807	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₁₄=0.712245	delAA=0.287755
Allele Frequency Aggregator	Total	Global	9996	(A)₁₄=0.8082	del(A)₄=0.0000, delAAA=0.0000, delAA=0.1786, delA=0.0132, dupA=0.0000
Allele Frequency Aggregator	European	Sub	7726	(A)₁₄=0.7523	del(A)₄=0.0000, delAAA=0.0000, delAA=0.2308, delA=0.0170, dupA=0.0000
Allele Frequency Aggregator	African	Sub	1624	(A)₁₄=1.0000	del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	252	(A)₁₄=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Other	Sub	240	(A)₁₄=0.988	del(A)₄=0.000, delAAA=0.000, delAA=0.008, delA=0.004, dupA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	74	(A)₁₄=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	South Asian	Sub	42	(A)₁₄=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Asian	Sub	38	(A)₁₄=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₄=0.6975	delAA=0.3025
1000Genomes	African	Sub	1322	(A)₁₄=0.7905	delAA=0.2095
1000Genomes	East Asian	Sub	1008	(A)₁₄=0.6012	delAA=0.3988
1000Genomes	Europe	Sub	1006	(A)₁₄=0.6750	delAA=0.3250
1000Genomes	South Asian	Sub	978	(A)₁₄=0.733	delAA=0.267
1000Genomes	American	Sub	694	(A)₁₄=0.643	delAA=0.357
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₄=0.65	delAA=0.35

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 7	NC_000007.14:g.9634266_9634269del
GRCh38.p14 chr 7	NC_000007.14:g.9634267_9634269del
GRCh38.p14 chr 7	NC_000007.14:g.9634268_9634269del
GRCh38.p14 chr 7	NC_000007.14:g.9634269del
GRCh38.p14 chr 7	NC_000007.14:g.9634269dup
GRCh38.p14 chr 7	NC_000007.14:g.9634268_9634269dup
GRCh37.p13 chr 7	NC_000007.13:g.9673896_9673899del
GRCh37.p13 chr 7	NC_000007.13:g.9673897_9673899del
GRCh37.p13 chr 7	NC_000007.13:g.9673898_9673899del
GRCh37.p13 chr 7	NC_000007.13:g.9673899del
GRCh37.p13 chr 7	NC_000007.13:g.9673899dup
GRCh37.p13 chr 7	NC_000007.13:g.9673898_9673899dup

Gene: PER3P1, PER3 pseudogene 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
PER3P1 transcript	NR_002790.3:n.	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)₁₄=	del(A)₄	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 7	NC_000007.14:g.9634256_9634269=	NC_000007.14:g.9634266_9634269del	NC_000007.14:g.9634267_9634269del	NC_000007.14:g.9634268_9634269del	NC_000007.14:g.9634269del	NC_000007.14:g.9634269dup	NC_000007.14:g.9634268_9634269dup
GRCh37.p13 chr 7	NC_000007.13:g.9673886_9673899=	NC_000007.13:g.9673896_9673899del	NC_000007.13:g.9673897_9673899del	NC_000007.13:g.9673898_9673899del	NC_000007.13:g.9673899del	NC_000007.13:g.9673899dup	NC_000007.13:g.9673898_9673899dup

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, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81700406	Dec 15, 2007 (129)
2	GMI	ss288822951	May 31, 2013 (142)
3	SSMP	ss663811120	Apr 01, 2015 (144)
4	1000GENOMES	ss1376739890	Aug 21, 2014 (142)
5	DDI	ss1536535779	Apr 01, 2015 (144)
6	EVA_GENOME_DK	ss1576937517	Apr 01, 2015 (144)
7	SWEGEN	ss3000593476	Nov 08, 2017 (151)
8	MCHAISSO	ss3065122331	Nov 08, 2017 (151)
9	EVA_DECODE	ss3719059331	Jul 13, 2019 (153)
10	EVA_DECODE	ss3719059332	Jul 13, 2019 (153)
11	EVA_DECODE	ss3719059333	Jul 13, 2019 (153)
12	EVA_DECODE	ss3719059334	Jul 13, 2019 (153)
13	ACPOP	ss3734337240	Jul 13, 2019 (153)
14	ACPOP	ss3734337241	Jul 13, 2019 (153)
15	INMEGENXS	ss3745689493	Jul 13, 2019 (153)
16	PACBIO	ss3785727979	Jul 13, 2019 (153)
17	PACBIO	ss3791042791	Jul 13, 2019 (153)
18	PACBIO	ss3795922478	Jul 13, 2019 (153)
19	KHV_HUMAN_GENOMES	ss3809326074	Jul 13, 2019 (153)
20	EVA	ss3830401421	Apr 26, 2020 (154)
21	KOGIC	ss3960850010	Apr 26, 2020 (154)
22	KOGIC	ss3960850011	Apr 26, 2020 (154)
23	KOGIC	ss3960850012	Apr 26, 2020 (154)
24	KOGIC	ss3960850013	Apr 26, 2020 (154)
25	FSA-LAB	ss3984360022	Apr 26, 2021 (155)
26	GNOMAD	ss4157998424	Apr 26, 2021 (155)
27	GNOMAD	ss4157998425	Apr 26, 2021 (155)
28	GNOMAD	ss4157998426	Apr 26, 2021 (155)
29	GNOMAD	ss4157998427	Apr 26, 2021 (155)
30	TOPMED	ss4734845897	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5181722013	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5181722014	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5181722015	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5181722016	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5271753105	Oct 13, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5271753106	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5271753107	Oct 13, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5271753108	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5469043858	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5469043859	Oct 13, 2022 (156)
41	EVA	ss5508837585	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5721152042	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5721152043	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5721152044	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5721152046	Oct 13, 2022 (156)
46	EVA	ss5822379261	Oct 13, 2022 (156)
47	EVA	ss5855751840	Oct 13, 2022 (156)
48	1000Genomes	NC_000007.13 - 9673886	Oct 12, 2018 (152)
49	The Danish reference pan genome	NC_000007.13 - 9673886	Apr 26, 2020 (154)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 252279303 (NC_000007.14:9634255::A 61/130418) Row 252279304 (NC_000007.14:9634255:A: 4532/130168) Row 252279305 (NC_000007.14:9634255:AA: 40049/130290)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 252279303 (NC_000007.14:9634255::A 61/130418) Row 252279304 (NC_000007.14:9634255:A: 4532/130168) Row 252279305 (NC_000007.14:9634255:AA: 40049/130290)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 252279303 (NC_000007.14:9634255::A 61/130418) Row 252279304 (NC_000007.14:9634255:A: 4532/130168) Row 252279305 (NC_000007.14:9634255:AA: 40049/130290)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 252279303 (NC_000007.14:9634255::A 61/130418) Row 252279304 (NC_000007.14:9634255:A: 4532/130168) Row 252279305 (NC_000007.14:9634255:AA: 40049/130290)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 252279303 (NC_000007.14:9634255::A 61/130418) Row 252279304 (NC_000007.14:9634255:A: 4532/130168) Row 252279305 (NC_000007.14:9634255:AA: 40049/130290)...	-	Apr 26, 2021 (155)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 17228011 (NC_000007.14:9634256:AA: 584/1832) Row 17228012 (NC_000007.14:9634257:A: 79/1832) Row 17228013 (NC_000007.14:9634258::A 25/1832)...	-	Apr 26, 2020 (154)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 17228011 (NC_000007.14:9634256:AA: 584/1832) Row 17228012 (NC_000007.14:9634257:A: 79/1832) Row 17228013 (NC_000007.14:9634258::A 25/1832)...	-	Apr 26, 2020 (154)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 17228011 (NC_000007.14:9634256:AA: 584/1832) Row 17228012 (NC_000007.14:9634257:A: 79/1832) Row 17228013 (NC_000007.14:9634258::A 25/1832)...	-	Apr 26, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 17228011 (NC_000007.14:9634256:AA: 584/1832) Row 17228012 (NC_000007.14:9634257:A: 79/1832) Row 17228013 (NC_000007.14:9634258::A 25/1832)...	-	Apr 26, 2020 (154)
59	Northern Sweden Submission ignored due to conflicting rows: Row 7622105 (NC_000007.13:9673885:AA: 242/600) Row 7622106 (NC_000007.13:9673885:A: 21/600)	-	Jul 13, 2019 (153)
60	Northern Sweden Submission ignored due to conflicting rows: Row 7622105 (NC_000007.13:9673885:AA: 242/600) Row 7622106 (NC_000007.13:9673885:A: 21/600)	-	Jul 13, 2019 (153)
61	8.3KJPN Submission ignored due to conflicting rows: Row 39691320 (NC_000007.13:9673885:AA: 4953/16758) Row 39691321 (NC_000007.13:9673885:A: 65/16758) Row 39691322 (NC_000007.13:9673885::A 13/16758)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 39691320 (NC_000007.13:9673885:AA: 4953/16758) Row 39691321 (NC_000007.13:9673885:A: 65/16758) Row 39691322 (NC_000007.13:9673885::A 13/16758)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 39691320 (NC_000007.13:9673885:AA: 4953/16758) Row 39691321 (NC_000007.13:9673885:A: 65/16758) Row 39691322 (NC_000007.13:9673885::A 13/16758)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 39691320 (NC_000007.13:9673885:AA: 4953/16758) Row 39691321 (NC_000007.13:9673885:A: 65/16758) Row 39691322 (NC_000007.13:9673885::A 13/16758)...	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 54989146 (NC_000007.14:9634255:AA: 8309/28254) Row 54989147 (NC_000007.14:9634255:A: 109/28254) Row 54989148 (NC_000007.14:9634255::A 23/28254)...	-	Oct 13, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 54989146 (NC_000007.14:9634255:AA: 8309/28254) Row 54989147 (NC_000007.14:9634255:A: 109/28254) Row 54989148 (NC_000007.14:9634255::A 23/28254)...	-	Oct 13, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 54989146 (NC_000007.14:9634255:AA: 8309/28254) Row 54989147 (NC_000007.14:9634255:A: 109/28254) Row 54989148 (NC_000007.14:9634255::A 23/28254)...	-	Oct 13, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 54989146 (NC_000007.14:9634255:AA: 8309/28254) Row 54989147 (NC_000007.14:9634255:A: 109/28254) Row 54989148 (NC_000007.14:9634255::A 23/28254)...	-	Oct 13, 2022 (156)
69	TopMed	NC_000007.14 - 9634256	Apr 26, 2021 (155)
70	ALFA	NC_000007.14 - 9634256	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)
rs386359626	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4157998427	NC_000007.14:9634255:AAAA:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAA	(self)
13464897603	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAA	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss5181722016	NC_000007.13:9673885:AAA:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3719059334, ss3960850013, ss4157998426, ss5271753108, ss5721152046	NC_000007.14:9634255:AAA:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
13464897603	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss288822951	NC_000007.12:9640410:AA:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
35767946, 1131429, ss663811120, ss1376739890, ss1536535779, ss1576937517, ss3000593476, ss3734337240, ss3745689493, ss3785727979, ss3791042791, ss3795922478, ss3830401421, ss3984360022, ss5181722013, ss5822379261	NC_000007.13:9673885:AA:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
572223456, ss3065122331, ss3809326074, ss4157998425, ss4734845897, ss5271753105, ss5469043858, ss5721152042, ss5855751840	NC_000007.14:9634255:AA:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
13464897603	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3719059333, ss3960850010	NC_000007.14:9634256:AA:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3734337241, ss5181722014	NC_000007.13:9673885:A:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5271753106, ss5469043859, ss5721152043	NC_000007.14:9634255:A:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
13464897603	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3719059332, ss3960850011	NC_000007.14:9634257:A:	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5181722015	NC_000007.13:9673885::A	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4157998424, ss5271753107, ss5721152044	NC_000007.14:9634255::A	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13464897603	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3719059331, ss3960850012	NC_000007.14:9634258::A	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5508837585	NC_000007.13:9673885::AA	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA
ss81700406	NT_007819.17:9663899::AA	NC_000007.14:9634255:AAAAAAAAAAAAA… NC_000007.14:9634255:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(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 rs60893428

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

rs60893428