Name: rs6602585
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.

rs6602585

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:6276974 (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>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.295629 (78250/264690, TOPMED)
C=0.210286 (29901/142192, ALFA)
C=0.290357 (40603/139838, GnomAD) (+ 16 more)
C=0.30648 (8660/28256, 14KJPN)
C=0.30698 (5145/16760, 8.3KJPN)
C=0.3171 (2031/6404, 1000G_30x)
C=0.3095 (1550/5008, 1000G)
C=0.1815 (813/4480, Estonian)
C=0.1975 (761/3854, ALSPAC)
C=0.1915 (710/3708, TWINSUK)
C=0.2461 (721/2930, KOREAN)
C=0.2282 (418/1832, Korea1K)
C=0.190 (190/998, GoNL)
C=0.177 (106/600, NorthernSweden)
C=0.173 (86/496, SGDP_PRJ)
C=0.371 (121/326, HapMap)
C=0.231 (50/216, Qatari)
C=0.11 (6/54, Siberian)
C=0.15 (6/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PFKFB3 : 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	142192	C=0.210286	T=0.789714
European	Sub	122718	C=0.196776	T=0.803224
African	Sub	5532	C=0.4958	T=0.5042
African Others	Sub	208	C=0.553	T=0.447
African American	Sub	5324	C=0.4936	T=0.5064
Asian	Sub	622	C=0.214	T=0.786
East Asian	Sub	490	C=0.210	T=0.790
Other Asian	Sub	132	C=0.227	T=0.773
Latin American 1	Sub	736	C=0.274	T=0.726
Latin American 2	Sub	6270	C=0.1981	T=0.8019
South Asian	Sub	184	C=0.234	T=0.766
Other	Sub	6130	C=0.2268	T=0.7732

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=0.295629	T=0.704371
Allele Frequency Aggregator	Total	Global	142192	C=0.210286	T=0.789714
Allele Frequency Aggregator	European	Sub	122718	C=0.196776	T=0.803224
Allele Frequency Aggregator	Latin American 2	Sub	6270	C=0.1981	T=0.8019
Allele Frequency Aggregator	Other	Sub	6130	C=0.2268	T=0.7732
Allele Frequency Aggregator	African	Sub	5532	C=0.4958	T=0.5042
Allele Frequency Aggregator	Latin American 1	Sub	736	C=0.274	T=0.726
Allele Frequency Aggregator	Asian	Sub	622	C=0.214	T=0.786
Allele Frequency Aggregator	South Asian	Sub	184	C=0.234	T=0.766
gnomAD - Genomes	Global	Study-wide	139838	C=0.290357	T=0.709643
gnomAD - Genomes	European	Sub	75812	C=0.19522	T=0.80478
gnomAD - Genomes	African	Sub	41818	C=0.50536	T=0.49464
gnomAD - Genomes	American	Sub	13622	C=0.20467	T=0.79533
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.1993	T=0.8007
gnomAD - Genomes	East Asian	Sub	3122	C=0.2040	T=0.7960
gnomAD - Genomes	Other	Sub	2142	C=0.2722	T=0.7278
14KJPN	JAPANESE	Study-wide	28256	C=0.30648	T=0.69352
8.3KJPN	JAPANESE	Study-wide	16760	C=0.30698	T=0.69302
1000Genomes_30x	Global	Study-wide	6404	C=0.3171	T=0.6829
1000Genomes_30x	African	Sub	1786	C=0.5616	T=0.4384
1000Genomes_30x	Europe	Sub	1266	C=0.2054	T=0.7946
1000Genomes_30x	South Asian	Sub	1202	C=0.2637	T=0.7363
1000Genomes_30x	East Asian	Sub	1170	C=0.2145	T=0.7855
1000Genomes_30x	American	Sub	980	C=0.204	T=0.796
1000Genomes	Global	Study-wide	5008	C=0.3095	T=0.6905
1000Genomes	African	Sub	1322	C=0.5416	T=0.4584
1000Genomes	East Asian	Sub	1008	C=0.2232	T=0.7768
1000Genomes	Europe	Sub	1006	C=0.2107	T=0.7893
1000Genomes	South Asian	Sub	978	C=0.262	T=0.738
1000Genomes	American	Sub	694	C=0.203	T=0.797
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.1815	T=0.8185
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.1975	T=0.8025
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.1915	T=0.8085
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.2461	G=0.0000, T=0.7539
Korean Genome Project	KOREAN	Study-wide	1832	C=0.2282	T=0.7718
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.190	T=0.810
Northern Sweden	ACPOP	Study-wide	600	C=0.177	T=0.823
SGDP_PRJ	Global	Study-wide	496	C=0.173	T=0.827
HapMap	Global	Study-wide	326	C=0.371	T=0.629
HapMap	African	Sub	120	C=0.592	T=0.408
HapMap	American	Sub	120	C=0.167	T=0.833
HapMap	Asian	Sub	86	C=0.35	T=0.65
Qatari	Global	Study-wide	216	C=0.231	T=0.769
Siberian	Global	Study-wide	54	C=0.11	T=0.89
The Danish reference pan genome	Danish	Study-wide	40	C=0.15	T=0.85

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 10	NC_000010.11:g.6276974C>G
GRCh38.p14 chr 10	NC_000010.11:g.6276974C>T
GRCh37.p13 chr 10	NC_000010.10:g.6318937C>G
GRCh37.p13 chr 10	NC_000010.10:g.6318937C>T

Gene: PFKFB3, 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PFKFB3 transcript variant 2	NM_001145443.3:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant 3	NM_001282630.3:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant 4	NM_001314063.2:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant 5	NM_001323016.2:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant 6	NM_001323017.2:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant 8	NM_001363545.2:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant 1	NM_004566.4:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant 7	NR_136554.2:n.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X2	XM_047425341.1:c.1456-495… XM_047425341.1:c.1456-49572C>G	N/A	Intron Variant
PFKFB3 transcript variant X8	XM_005252464.2:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X10	XM_011519493.2:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X1	XM_017016329.2:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X3	XM_047425342.1:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X4	XM_047425343.1:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X5	XM_047425344.1:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X6	XM_047425345.1:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X7	XM_047425346.1:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X9	XM_047425347.1:c.	N/A	Genic Downstream Transcript Variant
PFKFB3 transcript variant X11	XM_047425349.1:c.	N/A	Genic Downstream 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	C=	G	T
GRCh38.p14 chr 10	NC_000010.11:g.6276974=	NC_000010.11:g.6276974C>G	NC_000010.11:g.6276974C>T
GRCh37.p13 chr 10	NC_000010.10:g.6318937=	NC_000010.10:g.6318937C>G	NC_000010.10:g.6318937C>T
PFKFB3 transcript variant X2	XM_047425341.1:c.1456-49572=	XM_047425341.1:c.1456-49572C>G	XM_047425341.1:c.1456-49572C>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#.

111 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10643565	Jul 11, 2003 (116)
2	WI_SSAHASNP	ss12116551	Jul 11, 2003 (116)
3	SC_SNP	ss16090775	Feb 27, 2004 (120)
4	ILLUMINA	ss66784521	Nov 30, 2006 (127)
5	ILLUMINA	ss67478543	Nov 30, 2006 (127)
6	ILLUMINA	ss67834969	Nov 30, 2006 (127)
7	CSHL-HAPMAP	ss68398735	Jan 12, 2007 (127)
8	PERLEGEN	ss69068744	May 17, 2007 (127)
9	HGSV	ss77443259	Dec 06, 2007 (129)
10	HGSV	ss78313884	Dec 06, 2007 (129)
11	HGSV	ss82757811	Dec 16, 2007 (130)
12	HGSV	ss83418961	Dec 16, 2007 (130)
13	KRIBB_YJKIM	ss84514170	Dec 16, 2007 (130)
14	BCMHGSC_JDW	ss88080963	Mar 23, 2008 (129)
15	BGI	ss106653291	Feb 06, 2009 (130)
16	1000GENOMES	ss109197518	Jan 23, 2009 (130)
17	1000GENOMES	ss115305449	Jan 25, 2009 (130)
18	ILLUMINA-UK	ss119003966	Dec 01, 2009 (131)
19	ENSEMBL	ss131661883	Dec 01, 2009 (131)
20	ENSEMBL	ss143046219	Dec 01, 2009 (131)
21	GMI	ss154522829	Dec 01, 2009 (131)
22	ILLUMINA	ss160791812	Dec 01, 2009 (131)
23	COMPLETE_GENOMICS	ss167743479	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss168978964	Jul 04, 2010 (132)
25	COMPLETE_GENOMICS	ss170369480	Jul 04, 2010 (132)
26	1000GENOMES	ss224544574	Jul 14, 2010 (132)
27	1000GENOMES	ss235038108	Jul 15, 2010 (132)
28	1000GENOMES	ss241773924	Jul 15, 2010 (132)
29	BL	ss254025866	May 09, 2011 (134)
30	GMI	ss280464785	May 04, 2012 (137)
31	GMI	ss286122492	Apr 25, 2013 (138)
32	PJP	ss290900177	May 09, 2011 (134)
33	ILLUMINA	ss481298379	May 04, 2012 (137)
34	ILLUMINA	ss481323199	May 04, 2012 (137)
35	ILLUMINA	ss482305760	Sep 08, 2015 (146)
36	ILLUMINA	ss485444423	May 04, 2012 (137)
37	ILLUMINA	ss537370364	Sep 08, 2015 (146)
38	TISHKOFF	ss561745447	Apr 25, 2013 (138)
39	SSMP	ss656251677	Apr 25, 2013 (138)
40	ILLUMINA	ss779046188	Sep 08, 2015 (146)
41	ILLUMINA	ss783167664	Sep 08, 2015 (146)
42	ILLUMINA	ss784123289	Sep 08, 2015 (146)
43	ILLUMINA	ss832427141	Sep 08, 2015 (146)
44	ILLUMINA	ss834509096	Sep 08, 2015 (146)
45	EVA-GONL	ss987157373	Aug 21, 2014 (142)
46	JMKIDD_LAB	ss1076731757	Aug 21, 2014 (142)
47	1000GENOMES	ss1336130348	Aug 21, 2014 (142)
48	DDI	ss1426208865	Apr 01, 2015 (144)
49	EVA_GENOME_DK	ss1574889280	Apr 01, 2015 (144)
50	EVA_DECODE	ss1596805345	Apr 01, 2015 (144)
51	EVA_UK10K_ALSPAC	ss1623911893	Apr 01, 2015 (144)
52	EVA_UK10K_TWINSUK	ss1666905926	Apr 01, 2015 (144)
53	ILLUMINA	ss1751975133	Sep 08, 2015 (146)
54	HAMMER_LAB	ss1806238334	Sep 08, 2015 (146)
55	WEILL_CORNELL_DGM	ss1930478304	Feb 12, 2016 (147)
56	GENOMED	ss1967049574	Jul 19, 2016 (147)
57	JJLAB	ss2025962297	Sep 14, 2016 (149)
58	USC_VALOUEV	ss2154204326	Dec 20, 2016 (150)
59	HUMAN_LONGEVITY	ss2172358950	Dec 20, 2016 (150)
60	SYSTEMSBIOZJU	ss2627450055	Nov 08, 2017 (151)
61	ILLUMINA	ss2632669821	Nov 08, 2017 (151)
62	GRF	ss2698428241	Nov 08, 2017 (151)
63	GNOMAD	ss2885105798	Nov 08, 2017 (151)
64	SWEGEN	ss3005875718	Nov 08, 2017 (151)
65	BIOINF_KMB_FNS_UNIBA	ss3026764662	Nov 08, 2017 (151)
66	CSHL	ss3348941970	Nov 08, 2017 (151)
67	ILLUMINA	ss3626378190	Oct 12, 2018 (152)
68	ILLUMINA	ss3630697728	Oct 12, 2018 (152)
69	ILLUMINA	ss3632937002	Oct 12, 2018 (152)
70	ILLUMINA	ss3633633620	Oct 12, 2018 (152)
71	ILLUMINA	ss3634388409	Oct 12, 2018 (152)
72	ILLUMINA	ss3635326455	Oct 12, 2018 (152)
73	ILLUMINA	ss3636068226	Oct 12, 2018 (152)
74	ILLUMINA	ss3637077041	Oct 12, 2018 (152)
75	ILLUMINA	ss3638931208	Oct 12, 2018 (152)
76	ILLUMINA	ss3639464926	Oct 12, 2018 (152)
77	ILLUMINA	ss3640095757	Oct 12, 2018 (152)
78	URBANLAB	ss3649280478	Oct 12, 2018 (152)
79	EGCUT_WGS	ss3673402828	Jul 13, 2019 (153)
80	EVA_DECODE	ss3689206680	Jul 13, 2019 (153)
81	ACPOP	ss3737026985	Jul 13, 2019 (153)
82	ILLUMINA	ss3744689283	Jul 13, 2019 (153)
83	EVA	ss3747699748	Jul 13, 2019 (153)
84	ILLUMINA	ss3772189996	Jul 13, 2019 (153)
85	PACBIO	ss3786570225	Jul 13, 2019 (153)
86	PACBIO	ss3791764112	Jul 13, 2019 (153)
87	PACBIO	ss3796645892	Jul 13, 2019 (153)
88	KHV_HUMAN_GENOMES	ss3813062708	Jul 13, 2019 (153)
89	EVA	ss3831947063	Apr 26, 2020 (154)
90	EVA	ss3839504374	Apr 26, 2020 (154)
91	EVA	ss3844970358	Apr 26, 2020 (154)
92	SGDP_PRJ	ss3873453609	Apr 26, 2020 (154)
93	KRGDB	ss3921389081	Apr 26, 2020 (154)
94	KOGIC	ss3967131496	Apr 26, 2020 (154)
95	EVA	ss4017468493	Apr 26, 2021 (155)
96	TOPMED	ss4841244762	Apr 26, 2021 (155)
97	TOMMO_GENOMICS	ss5196097096	Apr 26, 2021 (155)
98	1000G_HIGH_COVERAGE	ss5282789443	Oct 16, 2022 (156)
99	EVA	ss5315448030	Oct 16, 2022 (156)
100	EVA	ss5391361333	Oct 16, 2022 (156)
101	HUGCELL_USP	ss5478580620	Oct 16, 2022 (156)
102	1000G_HIGH_COVERAGE	ss5576116712	Oct 16, 2022 (156)
103	SANFORD_IMAGENETICS	ss5648602018	Oct 16, 2022 (156)
104	TOMMO_GENOMICS	ss5740896450	Oct 16, 2022 (156)
105	EVA	ss5799802194	Oct 16, 2022 (156)
106	YY_MCH	ss5811162722	Oct 16, 2022 (156)
107	EVA	ss5823923374	Oct 16, 2022 (156)
108	EVA	ss5849420791	Oct 16, 2022 (156)
109	EVA	ss5877589916	Oct 16, 2022 (156)
110	EVA	ss5939883264	Oct 16, 2022 (156)
111	EVA	ss5980592505	Oct 16, 2022 (156)
112	1000Genomes	NC_000010.10 - 6318937	Oct 12, 2018 (152)
113	1000Genomes_30x	NC_000010.11 - 6276974	Oct 16, 2022 (156)
114	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 6318937	Oct 12, 2018 (152)
115	Genetic variation in the Estonian population	NC_000010.10 - 6318937	Oct 12, 2018 (152)
116	The Danish reference pan genome	NC_000010.10 - 6318937	Apr 26, 2020 (154)
117	gnomAD - Genomes	NC_000010.11 - 6276974	Apr 26, 2021 (155)
118	Genome of the Netherlands Release 5	NC_000010.10 - 6318937	Apr 26, 2020 (154)
119	HapMap	NC_000010.11 - 6276974	Apr 26, 2020 (154)
120	KOREAN population from KRGDB	NC_000010.10 - 6318937	Apr 26, 2020 (154)
121	Korean Genome Project	NC_000010.11 - 6276974	Apr 26, 2020 (154)
122	Northern Sweden	NC_000010.10 - 6318937	Jul 13, 2019 (153)
123	Qatari	NC_000010.10 - 6318937	Apr 26, 2020 (154)
124	SGDP_PRJ	NC_000010.10 - 6318937	Apr 26, 2020 (154)
125	Siberian	NC_000010.10 - 6318937	Apr 26, 2020 (154)
126	8.3KJPN	NC_000010.10 - 6318937	Apr 26, 2021 (155)
127	14KJPN	NC_000010.11 - 6276974	Oct 16, 2022 (156)
128	TopMed	NC_000010.11 - 6276974	Apr 26, 2021 (155)
129	UK 10K study - Twins	NC_000010.10 - 6318937	Oct 12, 2018 (152)
130	ALFA	NC_000010.11 - 6276974	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)
rs61391828	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
28566475, ss3921389081	NC_000010.10:6318936:C:G	NC_000010.11:6276973:C:G	(self)
ss77443259, ss78313884, ss82757811, ss83418961, ss3638931208, ss3639464926	NC_000010.8:6358942:C:T	NC_000010.11:6276973:C:T	(self)
ss88080963, ss109197518, ss115305449, ss119003966, ss167743479, ss168978964, ss170369480, ss254025866, ss280464785, ss286122492, ss290900177, ss481298379, ss1596805345	NC_000010.9:6358942:C:T	NC_000010.11:6276973:C:T	(self)
48471673, 26932316, 19141076, 2014483, 12012257, 28566475, 10311850, 12520234, 25470589, 6720680, 54066403, 26932316, ss224544574, ss235038108, ss241773924, ss481323199, ss482305760, ss485444423, ss537370364, ss561745447, ss656251677, ss779046188, ss783167664, ss784123289, ss832427141, ss834509096, ss987157373, ss1076731757, ss1336130348, ss1426208865, ss1574889280, ss1623911893, ss1666905926, ss1751975133, ss1806238334, ss1930478304, ss1967049574, ss2025962297, ss2154204326, ss2627450055, ss2632669821, ss2698428241, ss2885105798, ss3005875718, ss3348941970, ss3626378190, ss3630697728, ss3632937002, ss3633633620, ss3634388409, ss3635326455, ss3636068226, ss3637077041, ss3640095757, ss3673402828, ss3737026985, ss3744689283, ss3747699748, ss3772189996, ss3786570225, ss3791764112, ss3796645892, ss3831947063, ss3839504374, ss3873453609, ss3921389081, ss4017468493, ss5196097096, ss5315448030, ss5391361333, ss5648602018, ss5799802194, ss5823923374, ss5939883264, ss5980592505	NC_000010.10:6318936:C:T	NC_000010.11:6276973:C:T	(self)
63642647, 342417361, 330085, 23509497, 74733554, 56790417, 10235609986, ss2172358950, ss3026764662, ss3649280478, ss3689206680, ss3813062708, ss3844970358, ss3967131496, ss4841244762, ss5282789443, ss5478580620, ss5576116712, ss5740896450, ss5811162722, ss5849420791, ss5877589916	NC_000010.11:6276973:C:T	NC_000010.11:6276973:C:T	(self)
ss66784521, ss67478543, ss67834969, ss68398735, ss69068744, ss84514170, ss106653291, ss131661883, ss143046219, ss154522829, ss160791812	NT_008705.16:6258936:C:T	NC_000010.11:6276973:C:T	(self)
ss10643565, ss12116551, ss16090775	NT_077569.2:681832:C:T	NC_000010.11:6276973: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 rs6602585

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

rs6602585