Name: rs7698022
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.

rs7698022

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:55541180 (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: G>A / G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.226333 (59908/264690, TOPMED)
G=0.17093 (4830/28258, 14KJPN)
G=0.30943 (7380/23850, ALFA) (+ 15 more)
G=0.17208 (2884/16760, 8.3KJPN)
G=0.2277 (1458/6404, 1000G_30x)
G=0.2294 (1149/5008, 1000G)
G=0.3525 (1579/4480, Estonian)
G=0.2745 (1058/3854, ALSPAC)
G=0.2686 (996/3708, TWINSUK)
G=0.1007 (295/2930, KOREAN)
G=0.270 (269/998, GoNL)
G=0.257 (154/600, NorthernSweden)
G=0.185 (95/514, SGDP_PRJ)
G=0.213 (70/328, HapMap)
G=0.319 (69/216, Qatari)
G=0.093 (20/214, Vietnamese)
G=0.15 (8/52, Siberian)
G=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CLOCK : Intron Variant
Publications: 3 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	23850	G=0.30943	A=0.00000, T=0.69057
European	Sub	23088	G=0.30700	A=0.00000, T=0.69300
African	Sub	200	G=0.465	A=0.000, T=0.535
African Others	Sub	10	G=0.4	A=0.0, T=0.6
African American	Sub	190	G=0.468	A=0.000, T=0.532
Asian	Sub	48	G=0.08	A=0.00, T=0.92
East Asian	Sub	46	G=0.09	A=0.00, T=0.91
Other Asian	Sub	2	G=0.0	A=0.0, T=1.0
Latin American 1	Sub	8	G=1.0	A=0.0, T=0.0
Latin American 2	Sub	22	G=1.00	A=0.00, T=0.00
South Asian	Sub	20	G=0.85	A=0.00, T=0.15
Other	Sub	464	G=0.319	A=0.000, T=0.681

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	G=0.226333	T=0.773667
14KJPN	JAPANESE	Study-wide	28258	G=0.17093	T=0.82907
Allele Frequency Aggregator	Total	Global	23850	G=0.30943	A=0.00000, T=0.69057
Allele Frequency Aggregator	European	Sub	23088	G=0.30700	A=0.00000, T=0.69300
Allele Frequency Aggregator	Other	Sub	464	G=0.319	A=0.000, T=0.681
Allele Frequency Aggregator	African	Sub	200	G=0.465	A=0.000, T=0.535
Allele Frequency Aggregator	Asian	Sub	48	G=0.08	A=0.00, T=0.92
Allele Frequency Aggregator	Latin American 2	Sub	22	G=1.00	A=0.00, T=0.00
Allele Frequency Aggregator	South Asian	Sub	20	G=0.85	A=0.00, T=0.15
Allele Frequency Aggregator	Latin American 1	Sub	8	G=1.0	A=0.0, T=0.0
8.3KJPN	JAPANESE	Study-wide	16760	G=0.17208	T=0.82792
1000Genomes_30x	Global	Study-wide	6404	G=0.2277	T=0.7723
1000Genomes_30x	African	Sub	1786	G=0.1557	T=0.8443
1000Genomes_30x	Europe	Sub	1266	G=0.2994	T=0.7006
1000Genomes_30x	South Asian	Sub	1202	G=0.3810	T=0.6190
1000Genomes_30x	East Asian	Sub	1170	G=0.0974	T=0.9026
1000Genomes_30x	American	Sub	980	G=0.234	T=0.766
1000Genomes	Global	Study-wide	5008	G=0.2294	T=0.7706
1000Genomes	African	Sub	1322	G=0.1513	T=0.8487
1000Genomes	East Asian	Sub	1008	G=0.1012	T=0.8988
1000Genomes	Europe	Sub	1006	G=0.3052	T=0.6948
1000Genomes	South Asian	Sub	978	G=0.383	T=0.617
1000Genomes	American	Sub	694	G=0.238	T=0.762
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.3525	T=0.6475
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.2745	T=0.7255
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.2686	T=0.7314
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.1007	C=0.0000, T=0.8993
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.270	T=0.730
Northern Sweden	ACPOP	Study-wide	600	G=0.257	T=0.743
SGDP_PRJ	Global	Study-wide	514	G=0.185	T=0.815
HapMap	Global	Study-wide	328	G=0.213	T=0.787
HapMap	African	Sub	120	G=0.158	T=0.842
HapMap	American	Sub	120	G=0.275	T=0.725
HapMap	Asian	Sub	88	G=0.20	T=0.80
Qatari	Global	Study-wide	216	G=0.319	T=0.681
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.093	T=0.907
Siberian	Global	Study-wide	52	G=0.15	T=0.85
The Danish reference pan genome	Danish	Study-wide	40	G=0.20	T=0.80

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 4	NC_000004.12:g.55541180G>A
GRCh38.p14 chr 4	NC_000004.12:g.55541180G>C
GRCh38.p14 chr 4	NC_000004.12:g.55541180G>T
GRCh37.p13 chr 4	NC_000004.11:g.56407347G>A
GRCh37.p13 chr 4	NC_000004.11:g.56407347G>C
GRCh37.p13 chr 4	NC_000004.11:g.56407347G>T

Gene: CLOCK, clock circadian regulator (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CLOCK transcript variant 1	NM_001267843.2:c.-447+427… NM_001267843.2:c.-447+4273C>T	N/A	Intron Variant
CLOCK transcript variant 2	NM_004898.4:c.-290+5602C>T	N/A	Intron Variant
CLOCK transcript variant X1	XM_005265787.3:c.-290+530… XM_005265787.3:c.-290+5302C>T	N/A	Intron Variant
CLOCK transcript variant X4	XM_011534410.3:c.-136+560… XM_011534410.3:c.-136+5602C>T	N/A	Intron Variant
CLOCK transcript variant X5	XM_011534411.3:c.-136+530… XM_011534411.3:c.-136+5302C>T	N/A	Intron Variant
CLOCK transcript variant X3	XM_017008854.2:c.-447+560… XM_017008854.2:c.-447+5602C>T	N/A	Intron Variant
CLOCK transcript variant X7	XM_024454284.2:c.-290+449… XM_024454284.2:c.-290+4498C>T	N/A	Intron Variant
CLOCK transcript variant X2	XM_047416431.1:c.-447+530… XM_047416431.1:c.-447+5302C>T	N/A	Intron Variant
CLOCK transcript variant X6	XM_047416432.1:c.-293+560… XM_047416432.1:c.-293+5602C>T	N/A	Intron Variant
CLOCK transcript variant X8	XM_047416433.1:c.-3098+56… XM_047416433.1:c.-3098+5602C>T	N/A	Intron Variant
CLOCK transcript variant X9	XM_047416434.1:c.-3098+53… XM_047416434.1:c.-3098+5302C>T	N/A	Intron Variant
CLOCK transcript variant X10	XM_047416435.1:c.-352-494… XM_047416435.1:c.-352-4942C>T	N/A	Intron Variant
CLOCK transcript variant X11	XM_047416436.1:c.-2944+56… XM_047416436.1:c.-2944+5602C>T	N/A	Intron Variant
CLOCK transcript variant X12	XM_047416437.1:c.-2944+53… XM_047416437.1:c.-2944+5302C>T	N/A	Intron Variant
CLOCK transcript variant X13	XM_047416438.1:c.-290+427… XM_047416438.1:c.-290+4273C>T	N/A	Intron Variant
CLOCK transcript variant X14	XM_047416439.1:c.-293+530… XM_047416439.1:c.-293+5302C>T	N/A	Intron Variant
CLOCK transcript variant X15	XM_047416440.1:c.	N/A	Genic 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	G=	A	C	T
GRCh38.p14 chr 4	NC_000004.12:g.55541180=	NC_000004.12:g.55541180G>A	NC_000004.12:g.55541180G>C	NC_000004.12:g.55541180G>T
GRCh37.p13 chr 4	NC_000004.11:g.56407347=	NC_000004.11:g.56407347G>A	NC_000004.11:g.56407347G>C	NC_000004.11:g.56407347G>T
CLOCK transcript variant 1	NM_001267843.1:c.-447+4273=	NM_001267843.1:c.-447+4273C>T	NM_001267843.1:c.-447+4273C>G	NM_001267843.1:c.-447+4273C>A
CLOCK transcript variant 1	NM_001267843.2:c.-447+4273=	NM_001267843.2:c.-447+4273C>T	NM_001267843.2:c.-447+4273C>G	NM_001267843.2:c.-447+4273C>A
CLOCK transcript variant 2	NM_004898.3:c.-290+5602=	NM_004898.3:c.-290+5602C>T	NM_004898.3:c.-290+5602C>G	NM_004898.3:c.-290+5602C>A
CLOCK transcript variant 2	NM_004898.4:c.-290+5602=	NM_004898.4:c.-290+5602C>T	NM_004898.4:c.-290+5602C>G	NM_004898.4:c.-290+5602C>A
CLOCK transcript variant X1	XM_005265787.1:c.-290+5302=	XM_005265787.1:c.-290+5302C>T	XM_005265787.1:c.-290+5302C>G	XM_005265787.1:c.-290+5302C>A
CLOCK transcript variant X1	XM_005265787.3:c.-290+5302=	XM_005265787.3:c.-290+5302C>T	XM_005265787.3:c.-290+5302C>G	XM_005265787.3:c.-290+5302C>A
CLOCK transcript variant X4	XM_011534410.3:c.-136+5602=	XM_011534410.3:c.-136+5602C>T	XM_011534410.3:c.-136+5602C>G	XM_011534410.3:c.-136+5602C>A
CLOCK transcript variant X5	XM_011534411.3:c.-136+5302=	XM_011534411.3:c.-136+5302C>T	XM_011534411.3:c.-136+5302C>G	XM_011534411.3:c.-136+5302C>A
CLOCK transcript variant X3	XM_017008854.2:c.-447+5602=	XM_017008854.2:c.-447+5602C>T	XM_017008854.2:c.-447+5602C>G	XM_017008854.2:c.-447+5602C>A
CLOCK transcript variant X7	XM_024454284.2:c.-290+4498=	XM_024454284.2:c.-290+4498C>T	XM_024454284.2:c.-290+4498C>G	XM_024454284.2:c.-290+4498C>A
CLOCK transcript variant X2	XM_047416431.1:c.-447+5302=	XM_047416431.1:c.-447+5302C>T	XM_047416431.1:c.-447+5302C>G	XM_047416431.1:c.-447+5302C>A
CLOCK transcript variant X6	XM_047416432.1:c.-293+5602=	XM_047416432.1:c.-293+5602C>T	XM_047416432.1:c.-293+5602C>G	XM_047416432.1:c.-293+5602C>A
CLOCK transcript variant X8	XM_047416433.1:c.-3098+5602=	XM_047416433.1:c.-3098+5602C>T	XM_047416433.1:c.-3098+5602C>G	XM_047416433.1:c.-3098+5602C>A
CLOCK transcript variant X9	XM_047416434.1:c.-3098+5302=	XM_047416434.1:c.-3098+5302C>T	XM_047416434.1:c.-3098+5302C>G	XM_047416434.1:c.-3098+5302C>A
CLOCK transcript variant X10	XM_047416435.1:c.-352-4942=	XM_047416435.1:c.-352-4942C>T	XM_047416435.1:c.-352-4942C>G	XM_047416435.1:c.-352-4942C>A
CLOCK transcript variant X11	XM_047416436.1:c.-2944+5602=	XM_047416436.1:c.-2944+5602C>T	XM_047416436.1:c.-2944+5602C>G	XM_047416436.1:c.-2944+5602C>A
CLOCK transcript variant X12	XM_047416437.1:c.-2944+5302=	XM_047416437.1:c.-2944+5302C>T	XM_047416437.1:c.-2944+5302C>G	XM_047416437.1:c.-2944+5302C>A
CLOCK transcript variant X13	XM_047416438.1:c.-290+4273=	XM_047416438.1:c.-290+4273C>T	XM_047416438.1:c.-290+4273C>G	XM_047416438.1:c.-290+4273C>A
CLOCK transcript variant X14	XM_047416439.1:c.-293+5302=	XM_047416439.1:c.-293+5302C>T	XM_047416439.1:c.-293+5302C>G	XM_047416439.1:c.-293+5302C>A

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#.

72 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss11691381	Jul 11, 2003 (116)
2	ABI	ss42373383	Mar 14, 2006 (126)
3	HGSV	ss77173127	Dec 07, 2007 (129)
4	HGSV	ss81961782	Dec 14, 2007 (130)
5	BCMHGSC_JDW	ss92586742	Mar 24, 2008 (129)
6	HUMANGENOME_JCVI	ss98823953	Feb 03, 2009 (130)
7	BGI	ss104068071	Dec 01, 2009 (131)
8	KRIBB_YJKIM	ss104803475	Feb 03, 2009 (130)
9	1000GENOMES	ss112257899	Jan 25, 2009 (130)
10	1000GENOMES	ss113066679	Jan 25, 2009 (130)
11	ILLUMINA-UK	ss116993107	Feb 14, 2009 (130)
12	ENSEMBL	ss134694552	Dec 01, 2009 (131)
13	ENSEMBL	ss139616474	Dec 01, 2009 (131)
14	GMI	ss157268804	Dec 01, 2009 (131)
15	COMPLETE_GENOMICS	ss162117353	Jul 04, 2010 (132)
16	COMPLETE_GENOMICS	ss163449537	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss166588319	Jul 04, 2010 (132)
18	BUSHMAN	ss198515732	Jul 04, 2010 (132)
19	BCM-HGSC-SUB	ss206291191	Jul 04, 2010 (132)
20	1000GENOMES	ss220920877	Jul 14, 2010 (132)
21	1000GENOMES	ss232389274	Jul 14, 2010 (132)
22	1000GENOMES	ss239682878	Jul 15, 2010 (132)
23	GMI	ss277714897	May 04, 2012 (137)
24	GMI	ss284907721	Apr 25, 2013 (138)
25	PJP	ss293071205	May 09, 2011 (134)
26	TISHKOFF	ss557511639	Apr 25, 2013 (138)
27	SSMP	ss651307353	Apr 25, 2013 (138)
28	EVA-GONL	ss980105004	Aug 21, 2014 (142)
29	JMKIDD_LAB	ss1071529667	Aug 21, 2014 (142)
30	1000GENOMES	ss1309705398	Aug 21, 2014 (142)
31	DDI	ss1429880335	Apr 01, 2015 (144)
32	EVA_GENOME_DK	ss1580552093	Apr 01, 2015 (144)
33	EVA_DECODE	ss1589603126	Apr 01, 2015 (144)
34	EVA_UK10K_ALSPAC	ss1610071055	Apr 01, 2015 (144)
35	EVA_UK10K_TWINSUK	ss1653065088	Apr 01, 2015 (144)
36	HAMMER_LAB	ss1801435585	Sep 08, 2015 (146)
37	WEILL_CORNELL_DGM	ss1923344075	Feb 12, 2016 (147)
38	GENOMED	ss1969738039	Jul 19, 2016 (147)
39	JJLAB	ss2022255950	Sep 14, 2016 (149)
40	USC_VALOUEV	ss2150381119	Dec 20, 2016 (150)
41	HUMAN_LONGEVITY	ss2262887277	Dec 20, 2016 (150)
42	SYSTEMSBIOZJU	ss2625627246	Nov 08, 2017 (151)
43	GRF	ss2705846008	Nov 08, 2017 (151)
44	ILLUMINA	ss2711005055	Nov 08, 2017 (151)
45	GNOMAD	ss2809221971	Nov 08, 2017 (151)
46	SWEGEN	ss2994688121	Nov 08, 2017 (151)
47	BIOINF_KMB_FNS_UNIBA	ss3024899067	Nov 08, 2017 (151)
48	CSHL	ss3345710504	Nov 08, 2017 (151)
49	URBANLAB	ss3647727419	Oct 12, 2018 (152)
50	EGCUT_WGS	ss3662573794	Jul 13, 2019 (153)
51	EVA_DECODE	ss3712037869	Jul 13, 2019 (153)
52	ACPOP	ss3731141017	Jul 13, 2019 (153)
53	EVA	ss3761787740	Jul 13, 2019 (153)
54	KHV_HUMAN_GENOMES	ss3804923576	Jul 13, 2019 (153)
55	EVA	ss3828534663	Apr 26, 2020 (154)
56	EVA	ss3837704847	Apr 26, 2020 (154)
57	EVA	ss3843140955	Apr 26, 2020 (154)
58	SGDP_PRJ	ss3858929914	Apr 26, 2020 (154)
59	KRGDB	ss3905167878	Apr 26, 2020 (154)
60	TOPMED	ss4613617570	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5165682399	Apr 26, 2021 (155)
62	1000G_HIGH_COVERAGE	ss5259173769	Oct 13, 2022 (156)
63	EVA	ss5348960181	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5457938174	Oct 13, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5540227343	Oct 13, 2022 (156)
66	SANFORD_IMAGENETICS	ss5635012321	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5700018017	Oct 13, 2022 (156)
68	YY_MCH	ss5805075976	Oct 13, 2022 (156)
69	EVA	ss5843986336	Oct 13, 2022 (156)
70	EVA	ss5854217334	Oct 13, 2022 (156)
71	EVA	ss5863411683	Oct 13, 2022 (156)
72	EVA	ss5963386987	Oct 13, 2022 (156)
73	1000Genomes	NC_000004.11 - 56407347	Oct 12, 2018 (152)
74	1000Genomes_30x	NC_000004.12 - 55541180	Oct 13, 2022 (156)
75	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 56407347	Oct 12, 2018 (152)
76	Genetic variation in the Estonian population	NC_000004.11 - 56407347	Oct 12, 2018 (152)
77	The Danish reference pan genome	NC_000004.11 - 56407347	Apr 26, 2020 (154)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149551513 (NC_000004.12:55541179:G:A 2/140108) Row 149551514 (NC_000004.12:55541179:G:T 106118/140076)	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149551513 (NC_000004.12:55541179:G:A 2/140108) Row 149551514 (NC_000004.12:55541179:G:T 106118/140076)	-	Apr 26, 2021 (155)
80	Genome of the Netherlands Release 5	NC_000004.11 - 56407347	Apr 26, 2020 (154)
81	HapMap	NC_000004.12 - 55541180	Apr 26, 2020 (154)
82	KOREAN population from KRGDB	NC_000004.11 - 56407347	Apr 26, 2020 (154)
83	Northern Sweden	NC_000004.11 - 56407347	Jul 13, 2019 (153)
84	Qatari	NC_000004.11 - 56407347	Apr 26, 2020 (154)
85	SGDP_PRJ	NC_000004.11 - 56407347	Apr 26, 2020 (154)
86	Siberian	NC_000004.11 - 56407347	Apr 26, 2020 (154)
87	8.3KJPN	NC_000004.11 - 56407347	Apr 26, 2021 (155)
88	14KJPN	NC_000004.12 - 55541180	Oct 13, 2022 (156)
89	TopMed	NC_000004.12 - 55541180	Apr 26, 2021 (155)
90	UK 10K study - Twins	NC_000004.11 - 56407347	Oct 12, 2018 (152)
91	A Vietnamese Genetic Variation Database	NC_000004.11 - 56407347	Jul 13, 2019 (153)
92	ALFA	NC_000004.12 - 55541180	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)
rs57022688	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
8445422124	NC_000004.12:55541179:G:A	NC_000004.12:55541179:G:A	(self)
12345272, ss3905167878	NC_000004.11:56407346:G:C	NC_000004.12:55541179:G:C	(self)
ss77173127, ss81961782	NC_000004.9:56248274:G:T	NC_000004.12:55541179:G:T	(self)
ss92586742, ss112257899, ss113066679, ss116993107, ss162117353, ss163449537, ss166588319, ss198515732, ss206291191, ss277714897, ss284907721, ss293071205, ss1589603126	NC_000004.10:56102103:G:T	NC_000004.12:55541179:G:T	(self)
21099424, 11742843, 8312042, 6717032, 5177444, 12345272, 4425882, 5386005, 10946894, 2897473, 23651706, 11742843, 2578352, ss220920877, ss232389274, ss239682878, ss557511639, ss651307353, ss980105004, ss1071529667, ss1309705398, ss1429880335, ss1580552093, ss1610071055, ss1653065088, ss1801435585, ss1923344075, ss1969738039, ss2022255950, ss2150381119, ss2625627246, ss2705846008, ss2711005055, ss2809221971, ss2994688121, ss3345710504, ss3662573794, ss3731141017, ss3761787740, ss3828534663, ss3837704847, ss3858929914, ss3905167878, ss5165682399, ss5348960181, ss5635012321, ss5843986336, ss5963386987	NC_000004.11:56407346:G:T	NC_000004.12:55541179:G:T	(self)
27753278, 2614272, 33855121, 450995126, 8445422124, ss2262887277, ss3024899067, ss3647727419, ss3712037869, ss3804923576, ss3843140955, ss4613617570, ss5259173769, ss5457938174, ss5540227343, ss5700018017, ss5805075976, ss5854217334, ss5863411683	NC_000004.12:55541179:G:T	NC_000004.12:55541179:G:T	(self)
ss11691381	NT_022853.14:3747229:G:T	NC_000004.12:55541179:G:T	(self)
ss42373383, ss98823953, ss104068071, ss104803475, ss134694552, ss139616474, ss157268804	NT_022853.15:3747229:G:T	NC_000004.12:55541179:G:T	(self)

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

3 citations for rs7698022

PMID	Title	Author	Year	Journal
20124474	CLOCK in breast tumorigenesis: genetic, epigenetic, and transcriptional profiling analyses.	Hoffman AE et al.	2010	Cancer research
27313610	Evidences of Polymorphism Associated with Circadian System and Risk of Pathologies: A Review of the Literature.	Valenzuela FJ et al.	2016	International journal of endocrinology
31739444	Circadian Gene Polymorphisms Associated with Breast Cancer Susceptibility.	Lesicka M et al.	2019	International journal of molecular sciences

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

rs7698022