Name: rs73569323
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.

rs73569323

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:79211868 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.078027 (20653/264690, TOPMED)
T=0.046765 (9898/211654, GnomAD_exome)
T=0.079661 (11170/140220, GnomAD) (+ 21 more)
T=0.08943 (7031/78616, PAGE_STUDY)
T=0.06726 (4274/63548, ExAC)
T=0.05641 (2166/38400, ALFA)
T=0.04597 (1299/28258, 14KJPN)
T=0.04803 (805/16760, 8.3KJPN)
T=0.0782 (501/6404, 1000G_30x)
T=0.0779 (390/5008, 1000G)
T=0.0554 (248/4480, Estonian)
T=0.0426 (164/3854, ALSPAC)
T=0.0480 (178/3708, TWINSUK)
T=0.0311 (91/2922, KOREAN)
T=0.0349 (64/1832, Korea1K)
T=0.051 (51/998, GoNL)
T=0.032 (19/600, NorthernSweden)
T=0.024 (13/534, MGP)
T=0.083 (25/300, FINRISK)
T=0.037 (8/216, Qatari)
C=0.48 (30/62, SGDP_PRJ)
T=0.03 (1/40, GENOME_DK)
C=0.5 (4/8, Siberian)
T=0.5 (4/8, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: MAF : Non Coding Transcript Variant
WWOX : 3 Prime UTR 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	38494	C=0.94360	T=0.05640
European	Sub	27840	C=0.95266	T=0.04734
African	Sub	3864	C=0.8592	T=0.1408
African Others	Sub	122	C=0.803	T=0.197
African American	Sub	3742	C=0.8610	T=0.1390
Asian	Sub	224	C=0.978	T=0.022
East Asian	Sub	164	C=0.982	T=0.018
Other Asian	Sub	60	C=0.97	T=0.03
Latin American 1	Sub	162	C=0.969	T=0.031
Latin American 2	Sub	644	C=0.972	T=0.028
South Asian	Sub	120	C=0.950	T=0.050
Other	Sub	5640	C=0.9512	T=0.0488

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=0.921973	T=0.078027
gnomAD - Exomes	Global	Study-wide	211654	C=0.953235	T=0.046765
gnomAD - Exomes	European	Sub	110948	C=0.950698	T=0.049302
gnomAD - Exomes	Asian	Sub	43464	C=0.96958	T=0.03042
gnomAD - Exomes	American	Sub	30536	C=0.97960	T=0.02040
gnomAD - Exomes	African	Sub	12100	C=0.83711	T=0.16289
gnomAD - Exomes	Ashkenazi Jewish	Sub	9282	C=0.9662	T=0.0338
gnomAD - Exomes	Other	Sub	5324	C=0.9628	T=0.0372
gnomAD - Genomes	Global	Study-wide	140220	C=0.920339	T=0.079661
gnomAD - Genomes	European	Sub	75936	C=0.95048	T=0.04952
gnomAD - Genomes	African	Sub	42022	C=0.84311	T=0.15689
gnomAD - Genomes	American	Sub	13654	C=0.96214	T=0.03786
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.9702	T=0.0298
gnomAD - Genomes	East Asian	Sub	3132	C=0.9754	T=0.0246
gnomAD - Genomes	Other	Sub	2152	C=0.9424	T=0.0576
The PAGE Study	Global	Study-wide	78616	C=0.91057	T=0.08943
The PAGE Study	AfricanAmerican	Sub	32472	C=0.84556	T=0.15444
The PAGE Study	Mexican	Sub	10804	C=0.97936	T=0.02064
The PAGE Study	Asian	Sub	8304	C=0.9610	T=0.0390
The PAGE Study	PuertoRican	Sub	7908	C=0.9372	T=0.0628
The PAGE Study	NativeHawaiian	Sub	4530	C=0.9768	T=0.0232
The PAGE Study	Cuban	Sub	4228	C=0.9513	T=0.0487
The PAGE Study	Dominican	Sub	3826	C=0.8957	T=0.1043
The PAGE Study	CentralAmerican	Sub	2448	C=0.9608	T=0.0392
The PAGE Study	SouthAmerican	Sub	1982	C=0.9672	T=0.0328
The PAGE Study	NativeAmerican	Sub	1258	C=0.9412	T=0.0588
The PAGE Study	SouthAsian	Sub	856	C=0.968	T=0.032
ExAC	Global	Study-wide	63548	C=0.93274	T=0.06726
ExAC	Europe	Sub	37738	C=0.93545	T=0.06455
ExAC	Asian	Sub	15780	C=0.96185	T=0.03815
ExAC	African	Sub	5070	C=0.7931	T=0.2069
ExAC	American	Sub	4412	C=0.9653	T=0.0347
ExAC	Other	Sub	548	C=0.938	T=0.062
Allele Frequency Aggregator	Total	Global	38400	C=0.94359	T=0.05641
Allele Frequency Aggregator	European	Sub	27764	C=0.95267	T=0.04733
Allele Frequency Aggregator	Other	Sub	5622	C=0.9513	T=0.0487
Allele Frequency Aggregator	African	Sub	3864	C=0.8592	T=0.1408
Allele Frequency Aggregator	Latin American 2	Sub	644	C=0.972	T=0.028
Allele Frequency Aggregator	Asian	Sub	224	C=0.978	T=0.022
Allele Frequency Aggregator	Latin American 1	Sub	162	C=0.969	T=0.031
Allele Frequency Aggregator	South Asian	Sub	120	C=0.950	T=0.050
14KJPN	JAPANESE	Study-wide	28258	C=0.95403	T=0.04597
8.3KJPN	JAPANESE	Study-wide	16760	C=0.95197	T=0.04803
1000Genomes_30x	Global	Study-wide	6404	C=0.9218	T=0.0782
1000Genomes_30x	African	Sub	1786	C=0.8124	T=0.1876
1000Genomes_30x	Europe	Sub	1266	C=0.9487	T=0.0513
1000Genomes_30x	South Asian	Sub	1202	C=0.9684	T=0.0316
1000Genomes_30x	East Asian	Sub	1170	C=0.9752	T=0.0248
1000Genomes_30x	American	Sub	980	C=0.965	T=0.035
1000Genomes	Global	Study-wide	5008	C=0.9221	T=0.0779
1000Genomes	African	Sub	1322	C=0.8147	T=0.1853
1000Genomes	East Asian	Sub	1008	C=0.9722	T=0.0278
1000Genomes	Europe	Sub	1006	C=0.9433	T=0.0567
1000Genomes	South Asian	Sub	978	C=0.965	T=0.035
1000Genomes	American	Sub	694	C=0.963	T=0.037
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.9446	T=0.0554
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.9574	T=0.0426
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.9520	T=0.0480
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.9689	T=0.0311
Korean Genome Project	KOREAN	Study-wide	1832	C=0.9651	T=0.0349
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.949	T=0.051
Northern Sweden	ACPOP	Study-wide	600	C=0.968	T=0.032
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	C=0.976	T=0.024
FINRISK	Finnish from FINRISK project	Study-wide	300	C=0.917	T=0.083
Qatari	Global	Study-wide	216	C=0.963	T=0.037
SGDP_PRJ	Global	Study-wide	62	C=0.48	T=0.52
The Danish reference pan genome	Danish	Study-wide	40	C=0.97	T=0.03
Siberian	Global	Study-wide	8	C=0.5	T=0.5

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 16	NC_000016.10:g.79211868C>T
GRCh37.p13 chr 16	NC_000016.9:g.79245765C>T
WWOX RefSeqGene	NG_011698.1:g.1117215C>T

Gene: WWOX, WW domain containing oxidoreductase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
WWOX transcript variant 1	NM_016373.4:c.*72=	N/A	3 Prime UTR Variant
WWOX transcript variant 4	NM_001291997.2:c.*72=	N/A	3 Prime UTR Variant
WWOX transcript variant 2	NM_130791.5:c.	N/A	Genic Downstream Transcript Variant
WWOX transcript variant 3	NR_120435.2:n.	N/A	Genic Downstream Transcript Variant
WWOX transcript variant 5	NR_120436.3:n.	N/A	Genic Downstream Transcript Variant

Gene: MAF, MAF bZIP transcription factor (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAF transcript variant 2	NM_001031804.3:c.	N/A	Genic Downstream Transcript Variant
MAF transcript variant 1	NM_005360.5:c.	N/A	Genic Downstream Transcript Variant
MAF transcript variant X1	XM_024450279.2:c.*1062=	N/A	3 Prime UTR Variant
MAF transcript variant X7	XM_017023233.3:c.	N/A	Genic Downstream Transcript Variant
MAF transcript variant X6	XM_017023234.3:c.	N/A	Genic Downstream Transcript Variant
MAF transcript variant X8	XM_017023235.3:c.	N/A	Genic Downstream Transcript Variant
MAF transcript variant X2	XR_002957804.2:n.3049G>A	N/A	Non Coding Transcript Variant
MAF transcript variant X3	XR_002957802.2:n.3049G>A	N/A	Non Coding Transcript Variant
MAF transcript variant X4	XR_002957803.2:n.3049G>A	N/A	Non Coding Transcript Variant
MAF transcript variant X5	XR_001751902.3:n.3049G>A	N/A	Non Coding 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.

Allele: T (allele ID: 1285749 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001719172.1	not provided	Benign

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=	T
GRCh38.p14 chr 16	NC_000016.10:g.79211868=	NC_000016.10:g.79211868C>T
GRCh37.p13 chr 16	NC_000016.9:g.79245765=	NC_000016.9:g.79245765C>T
WWOX RefSeqGene	NG_011698.1:g.1117215=	NG_011698.1:g.1117215C>T
WWOX transcript variant 1	NM_016373.4:c.*72=	NM_016373.4:c.*72C>T
WWOX transcript variant 1	NM_016373.3:c.*72=	NM_016373.3:c.*72C>T
WWOX transcript variant 1	NM_016373.2:c.*72=	NM_016373.2:c.*72C>T
WWOX transcript variant 4	NM_001291997.2:c.*72=	NM_001291997.2:c.*72C>T
WWOX transcript variant 4	NM_001291997.1:c.*72=	NM_001291997.1:c.*72C>T
MAF transcript variant X5	XR_001751902.3:n.3049=	XR_001751902.3:n.3049G>A
MAF transcript variant X4	XR_001751902.2:n.4264=	XR_001751902.2:n.4264G>A
MAF transcript variant X1	XR_001751902.1:n.2721=	XR_001751902.1:n.2721G>A
MAF transcript variant X1	XM_024450279.2:c.*1062=	XM_024450279.2:c.*1062G>A
MAF transcript variant X1	XM_024450279.1:c.*1062=	XM_024450279.1:c.*1062G>A
MAF transcript variant X4	XR_002957803.2:n.3049=	XR_002957803.2:n.3049G>A
MAF transcript variant X3	XR_002957803.1:n.4264=	XR_002957803.1:n.4264G>A
MAF transcript variant X3	XR_002957802.2:n.3049=	XR_002957802.2:n.3049G>A
MAF transcript variant X2	XR_002957802.1:n.4264=	XR_002957802.1:n.4264G>A
MAF transcript variant X2	XR_002957804.2:n.3049=	XR_002957804.2:n.3049G>A
MAF transcript variant X5	XR_002957804.1:n.4264=	XR_002957804.1:n.4264G>A
WWOX transcript variant 4	NM_130788.1:c.*72=	NM_130788.1:c.*72C>T
WWOX transcript variant 5	NM_130792.1:c.*104=	NM_130792.1:c.*104C>T
WWOX transcript variant 3	NM_130790.1:c.670=	NM_130790.1:c.670C>T
HHCMA56 transcript	NM_004916.1:c.847=	NM_004916.1:c.847C>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#.

78 SubSNP, 23 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss115366091	Feb 14, 2009 (130)
2	ILLUMINA	ss161057540	Dec 01, 2009 (131)
3	COMPLETE_GENOMICS	ss170309447	Jul 04, 2010 (132)
4	COMPLETE_GENOMICS	ss171542164	Jul 04, 2010 (132)
5	BUSHMAN	ss201943567	Jul 04, 2010 (132)
6	1000GENOMES	ss227349057	Jul 14, 2010 (132)
7	1000GENOMES	ss237102019	Jul 15, 2010 (132)
8	ILLUMINA	ss479168522	Sep 08, 2015 (146)
9	CLINSEQ_SNP	ss491723145	May 04, 2012 (137)
10	TISHKOFF	ss565029725	Apr 25, 2013 (138)
11	SSMP	ss660809307	Apr 25, 2013 (138)
12	EVA-GONL	ss992706533	Aug 21, 2014 (142)
13	JMKIDD_LAB	ss1080778014	Aug 21, 2014 (142)
14	1000GENOMES	ss1357079990	Aug 21, 2014 (142)
15	EVA_GENOME_DK	ss1577999582	Apr 01, 2015 (144)
16	EVA_FINRISK	ss1584101459	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1634868345	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1677862378	Apr 01, 2015 (144)
19	EVA_EXAC	ss1692419848	Apr 01, 2015 (144)
20	EVA_DECODE	ss1696745561	Apr 01, 2015 (144)
21	EVA_MGP	ss1711436707	Apr 01, 2015 (144)
22	WEILL_CORNELL_DGM	ss1936137848	Feb 12, 2016 (147)
23	ILLUMINA	ss1959698956	Feb 12, 2016 (147)
24	JJLAB	ss2028856265	Sep 14, 2016 (149)
25	USC_VALOUEV	ss2157296790	Dec 20, 2016 (150)
26	HUMAN_LONGEVITY	ss2213880649	Dec 20, 2016 (150)
27	SYSTEMSBIOZJU	ss2628919718	Nov 08, 2017 (151)
28	GRF	ss2701829704	Nov 08, 2017 (151)
29	GNOMAD	ss2742167266	Nov 08, 2017 (151)
30	GNOMAD	ss2749598603	Nov 08, 2017 (151)
31	GNOMAD	ss2945416251	Nov 08, 2017 (151)
32	AFFY	ss2985075880	Nov 08, 2017 (151)
33	SWEGEN	ss3014854706	Nov 08, 2017 (151)
34	ILLUMINA	ss3021728037	Nov 08, 2017 (151)
35	BIOINF_KMB_FNS_UNIBA	ss3028244990	Nov 08, 2017 (151)
36	CSHL	ss3351546323	Nov 08, 2017 (151)
37	ILLUMINA	ss3636343342	Oct 12, 2018 (152)
38	OMUKHERJEE_ADBS	ss3646497986	Oct 12, 2018 (152)
39	ILLUMINA	ss3652139506	Oct 12, 2018 (152)
40	ILLUMINA	ss3653847724	Oct 12, 2018 (152)
41	EGCUT_WGS	ss3681833557	Jul 13, 2019 (153)
42	EVA_DECODE	ss3699673813	Jul 13, 2019 (153)
43	ILLUMINA	ss3725579793	Jul 13, 2019 (153)
44	ACPOP	ss3741688275	Jul 13, 2019 (153)
45	EVA	ss3754188837	Jul 13, 2019 (153)
46	PAGE_CC	ss3771893852	Jul 13, 2019 (153)
47	KHV_HUMAN_GENOMES	ss3819467713	Jul 13, 2019 (153)
48	EVA	ss3825883932	Apr 27, 2020 (154)
49	EVA	ss3834671469	Apr 27, 2020 (154)
50	SGDP_PRJ	ss3884877634	Apr 27, 2020 (154)
51	KRGDB	ss3934421283	Apr 27, 2020 (154)
52	KOGIC	ss3977995948	Apr 27, 2020 (154)
53	FSA-LAB	ss3984098813	Apr 27, 2021 (155)
54	EVA	ss3986696846	Apr 27, 2021 (155)
55	TOPMED	ss5022754577	Apr 27, 2021 (155)
56	TOMMO_GENOMICS	ss5220543198	Apr 27, 2021 (155)
57	EVA	ss5236935606	Apr 27, 2021 (155)
58	EVA	ss5237235463	Apr 27, 2021 (155)
59	EVA	ss5237567612	Apr 27, 2021 (155)
60	1000G_HIGH_COVERAGE	ss5301691338	Oct 17, 2022 (156)
61	EVA	ss5425064148	Oct 17, 2022 (156)
62	HUGCELL_USP	ss5494962358	Oct 17, 2022 (156)
63	EVA	ss5511675063	Oct 17, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5604723552	Oct 17, 2022 (156)
65	EVA	ss5624064681	Oct 17, 2022 (156)
66	SANFORD_IMAGENETICS	ss5624385660	Oct 17, 2022 (156)
67	SANFORD_IMAGENETICS	ss5659308600	Oct 17, 2022 (156)
68	TOMMO_GENOMICS	ss5775836519	Oct 17, 2022 (156)
69	YY_MCH	ss5816148937	Oct 17, 2022 (156)
70	EVA	ss5846694727	Oct 17, 2022 (156)
71	EVA	ss5847466333	Oct 17, 2022 (156)
72	EVA	ss5847778698	Oct 17, 2022 (156)
73	EVA	ss5848431030	Oct 17, 2022 (156)
74	EVA	ss5851650044	Oct 17, 2022 (156)
75	EVA	ss5899926069	Oct 17, 2022 (156)
76	EVA	ss5950716125	Oct 17, 2022 (156)
77	EVA	ss5979492061	Oct 17, 2022 (156)
78	EVA	ss5980933352	Oct 17, 2022 (156)
79	1000Genomes	NC_000016.9 - 79245765	Oct 12, 2018 (152)
80	1000Genomes_30x	NC_000016.10 - 79211868	Oct 17, 2022 (156)
81	The Avon Longitudinal Study of Parents and Children	NC_000016.9 - 79245765	Oct 12, 2018 (152)
82	Genetic variation in the Estonian population	NC_000016.9 - 79245765	Oct 12, 2018 (152)
83	ExAC	NC_000016.9 - 79245765	Oct 12, 2018 (152)
84	FINRISK	NC_000016.9 - 79245765	Apr 27, 2020 (154)
85	The Danish reference pan genome	NC_000016.9 - 79245765	Apr 27, 2020 (154)
86	gnomAD - Genomes	NC_000016.10 - 79211868	Apr 27, 2021 (155)
87	gnomAD - Exomes	NC_000016.9 - 79245765	Jul 13, 2019 (153)
88	Genome of the Netherlands Release 5	NC_000016.9 - 79245765	Apr 27, 2020 (154)
89	KOREAN population from KRGDB	NC_000016.9 - 79245765	Apr 27, 2020 (154)
90	Korean Genome Project	NC_000016.10 - 79211868	Apr 27, 2020 (154)
91	Medical Genome Project healthy controls from Spanish population	NC_000016.9 - 79245765	Apr 27, 2020 (154)
92	Northern Sweden	NC_000016.9 - 79245765	Jul 13, 2019 (153)
93	The PAGE Study	NC_000016.10 - 79211868	Jul 13, 2019 (153)
94	Qatari	NC_000016.9 - 79245765	Apr 27, 2020 (154)
95	SGDP_PRJ	NC_000016.9 - 79245765	Apr 27, 2020 (154)
96	Siberian	NC_000016.9 - 79245765	Apr 27, 2020 (154)
97	8.3KJPN	NC_000016.9 - 79245765	Apr 27, 2021 (155)
98	14KJPN	NC_000016.10 - 79211868	Oct 17, 2022 (156)
99	TopMed	NC_000016.10 - 79211868	Apr 27, 2021 (155)
100	UK 10K study - Twins	NC_000016.9 - 79245765	Oct 12, 2018 (152)
101	ALFA	NC_000016.10 - 79211868	Apr 27, 2021 (155)
102	ClinVar	RCV001719172.1	Oct 17, 2022 (156)

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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss115366091, ss170309447, ss171542164, ss201943567, ss491723145, ss1696745561	NC_000016.8:77803265:C:T	NC_000016.10:79211867:C:T	(self)
70270100, 38986187, 27571805, 2836016, 97920, 4208472, 11451440, 17380008, 41598677, 552467, 14973140, 18179770, 36894614, 9813144, 78512505, 38986187, ss227349057, ss237102019, ss479168522, ss565029725, ss660809307, ss992706533, ss1080778014, ss1357079990, ss1577999582, ss1584101459, ss1634868345, ss1677862378, ss1692419848, ss1711436707, ss1936137848, ss1959698956, ss2028856265, ss2157296790, ss2628919718, ss2701829704, ss2742167266, ss2749598603, ss2945416251, ss2985075880, ss3014854706, ss3021728037, ss3351546323, ss3636343342, ss3646497986, ss3652139506, ss3653847724, ss3681833557, ss3741688275, ss3754188837, ss3825883932, ss3834671469, ss3884877634, ss3934421283, ss3984098813, ss3986696846, ss5220543198, ss5237567612, ss5425064148, ss5511675063, ss5624064681, ss5624385660, ss5659308600, ss5846694727, ss5847466333, ss5847778698, ss5848431030, ss5950716125, ss5979492061, ss5980933352	NC_000016.9:79245764:C:T	NC_000016.10:79211867:C:T	(self)
RCV001719172.1, 92249487, 495737219, 34373949, 1115321, 109673623, 238300238, 10234088781, ss2213880649, ss3028244990, ss3699673813, ss3725579793, ss3771893852, ss3819467713, ss3977995948, ss5022754577, ss5236935606, ss5237235463, ss5301691338, ss5494962358, ss5604723552, ss5775836519, ss5816148937, ss5851650044, ss5899926069	NC_000016.10:79211867:C:T	NC_000016.10:79211867:C:T	(self)
ss161057540	NT_010498.15:32859963:C:T	NC_000016.10:79211867:C: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 rs73569323

PMID	Title	Author	Year	Journal
28426730	Functional genetic variant of WW domain-containing oxidoreductase (WWOX) gene is associated with hepatocellular carcinoma risk.	Lee HL et al.	2017	PloS one
30013442	Relationship of genetic variant distributions of WW domain-containing oxidoreductase gene with uterine cervical cancer.	Lin YH et al.	2018	International journal of medical sciences
34948746	Effect of WW Domain-Containing Oxidoreductase Gene Polymorphism on Clinicopathological Characteristics of Patients with EGFR Mutant Lung Adenocarcinoma in Taiwan.	Li JP et al.	2021	International journal of environmental research and public health

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs73569323