Name: rs60648502
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.

rs60648502

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:97146114-97146122 (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: delCC / delC / dupC / dupCC
Variation Type: Indel Insertion and Deletion
Frequency: delC=0.431849 (114306/264690, TOPMED)
delC=0.22946 (2413/10516, ALFA)
delC=0.4371 (2189/5008, 1000G) (+ 3 more)
delC=0.3671 (1566/4266, Estonian)
delC=0.3700 (1426/3854, ALSPAC)
delC=0.3708 (1375/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SDHAF3 : Intron Variant
LOC107984034 : 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	10516	CCCCCCCCC=0.76017	CCCCCCC=0.00000, CCCCCCCC=0.22946, CCCCCCCCCC=0.01037, CCCCCCCCCCC=0.00000	0.625121	0.088332	0.286546	32
European	Sub	9288	CCCCCCCCC=0.7345	CCCCCCC=0.0000, CCCCCCCC=0.2538, CCCCCCCCCC=0.0117, CCCCCCCCCCC=0.0000	0.584086	0.097642	0.318272	32
African	Sub	746	CCCCCCCCC=0.942	CCCCCCC=0.000, CCCCCCCC=0.058, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000	0.908847	0.024129	0.067024	29
African Others	Sub	36	CCCCCCCCC=0.92	CCCCCCC=0.00, CCCCCCCC=0.08, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00	0.833333	0.0	0.166667	0
African American	Sub	710	CCCCCCCCC=0.944	CCCCCCC=0.000, CCCCCCCC=0.056, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000	0.912676	0.025352	0.061972	33
Asian	Sub	30	CCCCCCCCC=0.93	CCCCCCC=0.00, CCCCCCCC=0.07, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00	0.933333	0.066667	0.0	9
East Asian	Sub	20	CCCCCCCCC=0.90	CCCCCCC=0.00, CCCCCCCC=0.10, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00	0.9	0.1	0.0	6
Other Asian	Sub	10	CCCCCCCCC=1.0	CCCCCCC=0.0, CCCCCCCC=0.0, CCCCCCCCCC=0.0, CCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	40	CCCCCCCCC=1.00	CCCCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	204	CCCCCCCCC=1.000	CCCCCCC=0.000, CCCCCCCC=0.000, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	24	CCCCCCCCC=1.00	CCCCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other	Sub	184	CCCCCCCCC=0.940	CCCCCCC=0.000, CCCCCCCC=0.060, CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000	0.902174	0.021739	0.076087	6

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	(C)₉=0.568151	delC=0.431849
Allele Frequency Aggregator	Total	Global	10516	(C)₉=0.76017	delCC=0.00000, delC=0.22946, dupC=0.01037, dupCC=0.00000
Allele Frequency Aggregator	European	Sub	9288	(C)₉=0.7345	delCC=0.0000, delC=0.2538, dupC=0.0117, dupCC=0.0000
Allele Frequency Aggregator	African	Sub	746	(C)₉=0.942	delCC=0.000, delC=0.058, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Latin American 2	Sub	204	(C)₉=1.000	delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Other	Sub	184	(C)₉=0.940	delCC=0.000, delC=0.060, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Latin American 1	Sub	40	(C)₉=1.00	delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
Allele Frequency Aggregator	Asian	Sub	30	(C)₉=0.93	delCC=0.00, delC=0.07, dupC=0.00, dupCC=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(C)₉=1.00	delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
1000Genomes	Global	Study-wide	5008	(C)₉=0.5629	delC=0.4371
1000Genomes	African	Sub	1322	(C)₉=0.4902	delC=0.5098
1000Genomes	East Asian	Sub	1008	(C)₉=0.5357	delC=0.4643
1000Genomes	Europe	Sub	1006	(C)₉=0.6501	delC=0.3499
1000Genomes	South Asian	Sub	978	(C)₉=0.575	delC=0.425
1000Genomes	American	Sub	694	(C)₉=0.598	delC=0.402
Genetic variation in the Estonian population	Estonian	Study-wide	4266	(C)₉=0.6329	delC=0.3671
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(C)₉=0.6300	delC=0.3700
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(C)₉=0.6292	delC=0.3708

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.97146121_97146122del
GRCh38.p14 chr 7	NC_000007.14:g.97146122del
GRCh38.p14 chr 7	NC_000007.14:g.97146122dup
GRCh38.p14 chr 7	NC_000007.14:g.97146121_97146122dup
GRCh37.p13 chr 7	NC_000007.13:g.96775433_96775434del
GRCh37.p13 chr 7	NC_000007.13:g.96775434del
GRCh37.p13 chr 7	NC_000007.13:g.96775434dup
GRCh37.p13 chr 7	NC_000007.13:g.96775433_96775434dup

Gene: SDHAF3, succinate dehydrogenase complex assembly factor 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SDHAF3 transcript	NM_020186.3:c.174+28224_1… NM_020186.3:c.174+28224_174+28225del	N/A	Intron Variant

Gene: LOC107984034, uncharacterized LOC107984034 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107984034 transcript	XR_001745291.1: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)₉=	delCC	delC	dupC	dupCC
GRCh38.p14 chr 7	NC_000007.14:g.97146114_97146122=	NC_000007.14:g.97146121_97146122del	NC_000007.14:g.97146122del	NC_000007.14:g.97146122dup	NC_000007.14:g.97146121_97146122dup
GRCh37.p13 chr 7	NC_000007.13:g.96775426_96775434=	NC_000007.13:g.96775433_96775434del	NC_000007.13:g.96775434del	NC_000007.13:g.96775434dup	NC_000007.13:g.96775433_96775434dup
SDHAF3 transcript	NM_020186.2:c.174+28217=	NM_020186.2:c.174+28224_174+28225del	NM_020186.2:c.174+28225del	NM_020186.2:c.174+28225dup	NM_020186.2:c.174+28224_174+28225dup
SDHAF3 transcript	NM_020186.3:c.174+28217=	NM_020186.3:c.174+28224_174+28225del	NM_020186.3:c.174+28225del	NM_020186.3:c.174+28225dup	NM_020186.3:c.174+28224_174+28225dup

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#.

57 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80102069	Sep 08, 2015 (146)
2	BGI	ss104778754	Dec 06, 2013 (138)
3	BUSHMAN	ss193934912	Jul 04, 2010 (137)
4	GMI	ss287817146	May 09, 2011 (134)
5	GMI	ss288859936	May 04, 2012 (137)
6	1000GENOMES	ss326966533	May 09, 2011 (137)
7	1000GENOMES	ss327020922	May 09, 2011 (137)
8	1000GENOMES	ss327315784	May 09, 2011 (137)
9	LUNTER	ss551764404	Apr 25, 2013 (138)
10	LUNTER	ss551968607	Apr 25, 2013 (138)
11	LUNTER	ss553309347	Apr 25, 2013 (138)
12	SSMP	ss663811145	Apr 01, 2015 (144)
13	BILGI_BIOE	ss666408973	Apr 25, 2013 (138)
14	1000GENOMES	ss1377405364	Aug 21, 2014 (142)
15	DDI	ss1536556546	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1705742059	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1705742135	Apr 01, 2015 (144)
18	HAMMER_LAB	ss1805125595	Sep 08, 2015 (146)
19	SYSTEMSBIOZJU	ss2626791692	Nov 08, 2017 (151)
20	MCHAISSO	ss3065149015	Nov 08, 2017 (151)
21	BEROUKHIMLAB	ss3644244284	Oct 12, 2018 (152)
22	BIOINF_KMB_FNS_UNIBA	ss3646045490	Oct 12, 2018 (152)
23	EGCUT_WGS	ss3669436632	Jul 13, 2019 (153)
24	EVA_DECODE	ss3720263609	Jul 13, 2019 (153)
25	EVA_DECODE	ss3720263610	Jul 13, 2019 (153)
26	ACPOP	ss3734886542	Jul 13, 2019 (153)
27	ACPOP	ss3734886543	Jul 13, 2019 (153)
28	PACBIO	ss3785900392	Jul 13, 2019 (153)
29	PACBIO	ss3791189657	Jul 13, 2019 (153)
30	PACBIO	ss3796069646	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3810075808	Jul 13, 2019 (153)
32	EVA	ss3830713424	Apr 26, 2020 (154)
33	EVA	ss3838855723	Apr 26, 2020 (154)
34	EVA	ss3844310764	Apr 26, 2020 (154)
35	KOGIC	ss3962147854	Apr 26, 2020 (154)
36	KOGIC	ss3962147855	Apr 26, 2020 (154)
37	GNOMAD	ss4169049645	Apr 26, 2021 (155)
38	GNOMAD	ss4169049646	Apr 26, 2021 (155)
39	GNOMAD	ss4169049647	Apr 26, 2021 (155)
40	GNOMAD	ss4169049648	Apr 26, 2021 (155)
41	TOPMED	ss4755951648	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5184574571	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5184574572	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5184574573	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5273965279	Oct 13, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5273965280	Oct 13, 2022 (156)
47	HUGCELL_USP	ss5470944820	Oct 13, 2022 (156)
48	HUGCELL_USP	ss5470944821	Oct 13, 2022 (156)
49	HUGCELL_USP	ss5470944822	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5725256074	Oct 13, 2022 (156)
51	TOMMO_GENOMICS	ss5725256075	Oct 13, 2022 (156)
52	TOMMO_GENOMICS	ss5725256076	Oct 13, 2022 (156)
53	YY_MCH	ss5808909514	Oct 13, 2022 (156)
54	EVA	ss5823230304	Oct 13, 2022 (156)
55	EVA	ss5856014875	Oct 13, 2022 (156)
56	EVA	ss5860015505	Oct 13, 2022 (156)
57	EVA	ss5972735119	Oct 13, 2022 (156)
58	1000Genomes	NC_000007.13 - 96775426	Oct 12, 2018 (152)
59	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 96775426	Oct 12, 2018 (152)
60	Genetic variation in the Estonian population	NC_000007.13 - 96775426	Oct 12, 2018 (152)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270104524 (NC_000007.14:97146113::C 2784/139170) Row 270104525 (NC_000007.14:97146113::CC 1/139224) Row 270104526 (NC_000007.14:97146113:C: 58742/139132)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270104524 (NC_000007.14:97146113::C 2784/139170) Row 270104525 (NC_000007.14:97146113::CC 1/139224) Row 270104526 (NC_000007.14:97146113:C: 58742/139132)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270104524 (NC_000007.14:97146113::C 2784/139170) Row 270104525 (NC_000007.14:97146113::CC 1/139224) Row 270104526 (NC_000007.14:97146113:C: 58742/139132)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270104524 (NC_000007.14:97146113::C 2784/139170) Row 270104525 (NC_000007.14:97146113::CC 1/139224) Row 270104526 (NC_000007.14:97146113:C: 58742/139132)...	-	Apr 26, 2021 (155)
65	Korean Genome Project Submission ignored due to conflicting rows: Row 18525855 (NC_000007.14:97146113:C: 925/1832) Row 18525856 (NC_000007.14:97146114::C 3/1832)	-	Apr 26, 2020 (154)
66	Korean Genome Project Submission ignored due to conflicting rows: Row 18525855 (NC_000007.14:97146113:C: 925/1832) Row 18525856 (NC_000007.14:97146114::C 3/1832)	-	Apr 26, 2020 (154)
67	Northern Sweden Submission ignored due to conflicting rows: Row 8171407 (NC_000007.13:96775425:C: 241/600) Row 8171408 (NC_000007.13:96775425::C 20/600)	-	Jul 13, 2019 (153)
68	Northern Sweden Submission ignored due to conflicting rows: Row 8171407 (NC_000007.13:96775425:C: 241/600) Row 8171408 (NC_000007.13:96775425::C 20/600)	-	Jul 13, 2019 (153)
69	8.3KJPN Submission ignored due to conflicting rows: Row 42543878 (NC_000007.13:96775425:C: 8682/16758) Row 42543879 (NC_000007.13:96775425::C 59/16758) Row 42543880 (NC_000007.13:96775425:CC: 3/16758)	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 42543878 (NC_000007.13:96775425:C: 8682/16758) Row 42543879 (NC_000007.13:96775425::C 59/16758) Row 42543880 (NC_000007.13:96775425:CC: 3/16758)	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 42543878 (NC_000007.13:96775425:C: 8682/16758) Row 42543879 (NC_000007.13:96775425::C 59/16758) Row 42543880 (NC_000007.13:96775425:CC: 3/16758)	-	Apr 26, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 59093178 (NC_000007.14:97146113:C: 14618/28258) Row 59093179 (NC_000007.14:97146113::C 92/28258) Row 59093180 (NC_000007.14:97146113:CC: 6/28258)	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 59093178 (NC_000007.14:97146113:C: 14618/28258) Row 59093179 (NC_000007.14:97146113::C 92/28258) Row 59093180 (NC_000007.14:97146113:CC: 6/28258)	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 59093178 (NC_000007.14:97146113:C: 14618/28258) Row 59093179 (NC_000007.14:97146113::C 92/28258) Row 59093180 (NC_000007.14:97146113:CC: 6/28258)	-	Oct 13, 2022 (156)
75	TopMed	NC_000007.14 - 97146114	Apr 26, 2021 (155)
76	UK 10K study - Twins	NC_000007.13 - 96775426	Oct 12, 2018 (152)
77	ALFA	NC_000007.14 - 97146114	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)
rs66470332	May 11, 2012 (137)
rs77066782	May 11, 2012 (137)
rs143203898	May 04, 2012 (137)
rs370298653	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5184574573	NC_000007.13:96775425:CC:	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCC	(self)
ss4169049648, ss5470944822, ss5725256076	NC_000007.14:97146113:CC:	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCC	(self)
11189606432	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCC	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCC	(self)
ss80102069	NC_000007.11:96420084:C:	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCC	(self)
ss288859936, ss326966533, ss327020922, ss327315784, ss551764404, ss551968607, ss553309347	NC_000007.12:96613361:C:	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCC	(self)
38277757, 21301157, 15174880, 21301157, ss663811145, ss666408973, ss1377405364, ss1536556546, ss1705742059, ss1705742135, ss1805125595, ss2626791692, ss3644244284, ss3669436632, ss3734886542, ss3785900392, ss3791189657, ss3796069646, ss3830713424, ss3838855723, ss5184574571, ss5823230304, ss5972735119	NC_000007.13:96775425:C:	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCC	(self)
593329207, ss3065149015, ss3646045490, ss3720263610, ss3810075808, ss3844310764, ss3962147854, ss4169049647, ss4755951648, ss5273965279, ss5470944820, ss5725256074, ss5808909514, ss5856014875, ss5860015505	NC_000007.14:97146113:C:	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCC	(self)
11189606432	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCC	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCC	(self)
ss104778754	NT_007933.15:34808275:C:	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCC	(self)
ss193934912	NT_007933.16:34639334:C:	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCC	(self)
ss3734886543, ss5184574572	NC_000007.13:96775425::C	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCC	(self)
ss4169049645, ss5273965280, ss5470944821, ss5725256075	NC_000007.14:97146113::C	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCC	(self)
11189606432	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCC	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCC	(self)
ss3720263609, ss3962147855	NC_000007.14:97146114::C	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCC	(self)
ss287817146	NT_007933.15:34808277::C	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCC	(self)
ss4169049646	NC_000007.14:97146113::CC	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCCC	(self)
11189606432	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCCC	NC_000007.14:97146113:CCCCCCCCC:CC… NC_000007.14:97146113:CCCCCCCCC:CCCCCCCCCCC	(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 rs60648502

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

rs60648502