Name: rs220207
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.

rs220207

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr21:42019511 (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: A>C / A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.433549 (114756/264690, TOPMED)
G=0.493129 (61504/124722, ALFA)
G=0.14679 (4148/28258, 14KJPN) (+ 15 more)
G=0.14409 (2415/16760, 8.3KJPN)
G=0.3780 (2421/6404, 1000G_30x)
G=0.3786 (1896/5008, 1000G)
G=0.4877 (2185/4480, Estonian)
G=0.1126 (330/2930, KOREAN)
G=0.3490 (726/2080, HGDP_Stanford)
G=0.3176 (597/1880, HapMap)
A=0.486 (485/998, GoNL)
G=0.495 (297/600, NorthernSweden)
A=0.350 (96/274, SGDP_PRJ)
G=0.398 (86/216, Qatari)
G=0.152 (32/210, Vietnamese)
A=0.44 (28/64, Ancient Sardinia)
A=0.40 (16/40, GENOME_DK)
A=0.34 (13/38, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF295-AS1 : 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	124722	A=0.506871	C=0.000000, G=0.493129
European	Sub	101962	A=0.483278	C=0.000000, G=0.516722
African	Sub	5316	A=0.7406	C=0.0000, G=0.2594
African Others	Sub	200	A=0.780	C=0.000, G=0.220
African American	Sub	5116	A=0.7391	C=0.0000, G=0.2609
Asian	Sub	634	A=0.901	C=0.000, G=0.099
East Asian	Sub	512	A=0.912	C=0.000, G=0.088
Other Asian	Sub	122	A=0.852	C=0.000, G=0.148
Latin American 1	Sub	670	A=0.536	C=0.000, G=0.464
Latin American 2	Sub	5944	A=0.6351	C=0.0000, G=0.3649
South Asian	Sub	4972	A=0.5177	C=0.0000, G=0.4823
Other	Sub	5224	A=0.5218	C=0.0000, G=0.4782

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	A=0.566451	G=0.433549
Allele Frequency Aggregator	Total	Global	124722	A=0.506871	C=0.000000, G=0.493129
Allele Frequency Aggregator	European	Sub	101962	A=0.483278	C=0.000000, G=0.516722
Allele Frequency Aggregator	Latin American 2	Sub	5944	A=0.6351	C=0.0000, G=0.3649
Allele Frequency Aggregator	African	Sub	5316	A=0.7406	C=0.0000, G=0.2594
Allele Frequency Aggregator	Other	Sub	5224	A=0.5218	C=0.0000, G=0.4782
Allele Frequency Aggregator	South Asian	Sub	4972	A=0.5177	C=0.0000, G=0.4823
Allele Frequency Aggregator	Latin American 1	Sub	670	A=0.536	C=0.000, G=0.464
Allele Frequency Aggregator	Asian	Sub	634	A=0.901	C=0.000, G=0.099
14KJPN	JAPANESE	Study-wide	28258	A=0.85321	G=0.14679
8.3KJPN	JAPANESE	Study-wide	16760	A=0.85591	G=0.14409
1000Genomes_30x	Global	Study-wide	6404	A=0.6220	G=0.3780
1000Genomes_30x	African	Sub	1786	A=0.6781	G=0.3219
1000Genomes_30x	Europe	Sub	1266	A=0.4676	G=0.5324
1000Genomes_30x	South Asian	Sub	1202	A=0.4908	G=0.5092
1000Genomes_30x	East Asian	Sub	1170	A=0.8735	G=0.1265
1000Genomes_30x	American	Sub	980	A=0.580	G=0.420
1000Genomes	Global	Study-wide	5008	A=0.6214	G=0.3786
1000Genomes	African	Sub	1322	A=0.6725	G=0.3275
1000Genomes	East Asian	Sub	1008	A=0.8730	G=0.1270
1000Genomes	Europe	Sub	1006	A=0.4682	G=0.5318
1000Genomes	South Asian	Sub	978	A=0.481	G=0.519
1000Genomes	American	Sub	694	A=0.579	G=0.421
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.5123	G=0.4877
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.8874	G=0.1126
HGDP-CEPH-db Supplement 1	Global	Study-wide	2080	A=0.6510	G=0.3490
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.836	G=0.164
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.522	G=0.478
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.551	G=0.449
HGDP-CEPH-db Supplement 1	Europe	Sub	318	A=0.481	G=0.519
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.764	G=0.236
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.676	G=0.324
HGDP-CEPH-db Supplement 1	Oceania	Sub	70	A=0.97	G=0.03
HapMap	Global	Study-wide	1880	A=0.6824	G=0.3176
HapMap	American	Sub	762	A=0.631	G=0.369
HapMap	African	Sub	688	A=0.718	G=0.282
HapMap	Asian	Sub	254	A=0.890	G=0.110
HapMap	Europe	Sub	176	A=0.466	G=0.534
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.486	G=0.514
Northern Sweden	ACPOP	Study-wide	600	A=0.505	G=0.495
SGDP_PRJ	Global	Study-wide	274	A=0.350	G=0.650
Qatari	Global	Study-wide	216	A=0.602	G=0.398
A Vietnamese Genetic Variation Database	Global	Study-wide	210	A=0.848	G=0.152
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	64	A=0.44	G=0.56
The Danish reference pan genome	Danish	Study-wide	40	A=0.40	G=0.60
Siberian	Global	Study-wide	38	A=0.34	G=0.66

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 21	NC_000021.9:g.42019511A>C
GRCh38.p14 chr 21	NC_000021.9:g.42019511A>G
GRCh37.p13 chr 21	NC_000021.8:g.43439620A>C
GRCh37.p13 chr 21	NC_000021.8:g.43439620A>G

Gene: ZNF295-AS1, ZNF295 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF295-AS1 transcript variant 1	NR_119384.1:n.	N/A	Intron Variant
ZNF295-AS1 transcript variant 3	NR_027273.2:n.	N/A	Genic Upstream Transcript Variant
ZNF295-AS1 transcript variant 2	NR_119385.1:n.	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	A=	C	G
GRCh38.p14 chr 21	NC_000021.9:g.42019511=	NC_000021.9:g.42019511A>C	NC_000021.9:g.42019511A>G
GRCh37.p13 chr 21	NC_000021.8:g.43439620=	NC_000021.8:g.43439620A>C	NC_000021.8:g.43439620A>G

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#.

115 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KWOK	ss286493	Jul 12, 2000 (79)
2	SC_JCM	ss472656	Jul 16, 2000 (80)
3	KWOK	ss1240583	Oct 05, 2000 (92)
4	KWOK	ss1837477	Oct 18, 2000 (92)
5	BCM_SSAHASNP	ss10992787	Jul 11, 2003 (116)
6	WUGSC_SSAHASNP	ss14439556	Dec 05, 2003 (119)
7	CSHL-HAPMAP	ss16911160	Feb 27, 2004 (120)
8	SSAHASNP	ss21835691	Apr 05, 2004 (121)
9	ABI	ss44257734	Mar 14, 2006 (126)
10	ILLUMINA	ss67233296	Dec 01, 2006 (127)
11	ILLUMINA	ss67629079	Dec 01, 2006 (127)
12	ILLUMINA	ss68198969	Dec 12, 2006 (127)
13	PERLEGEN	ss69255191	May 17, 2007 (127)
14	ILLUMINA	ss70711634	May 26, 2008 (130)
15	ILLUMINA	ss71279003	May 17, 2007 (127)
16	ILLUMINA	ss75650938	Dec 07, 2007 (129)
17	HGSV	ss80891191	Dec 15, 2007 (130)
18	KRIBB_YJKIM	ss83391143	Dec 15, 2007 (130)
19	BCMHGSC_JDW	ss91849900	Mar 24, 2008 (129)
20	HUMANGENOME_JCVI	ss96172132	Feb 06, 2009 (130)
21	ILLUMINA-UK	ss117538460	Feb 14, 2009 (130)
22	ENSEMBL	ss135595779	Dec 01, 2009 (131)
23	ENSEMBL	ss138322562	Dec 01, 2009 (131)
24	ILLUMINA	ss153881068	Dec 01, 2009 (131)
25	ILLUMINA	ss159367727	Dec 01, 2009 (131)
26	ILLUMINA	ss160513975	Dec 01, 2009 (131)
27	COMPLETE_GENOMICS	ss168105418	Jul 04, 2010 (132)
28	ILLUMINA	ss173176207	Jul 04, 2010 (132)
29	BUSHMAN	ss204028090	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss208800959	Jul 04, 2010 (132)
31	1000GENOMES	ss212091925	Jul 14, 2010 (132)
32	1000GENOMES	ss228584198	Jul 14, 2010 (132)
33	1000GENOMES	ss237996467	Jul 15, 2010 (132)
34	1000GENOMES	ss244132403	Jul 15, 2010 (132)
35	BL	ss255986803	May 09, 2011 (134)
36	PJP	ss292717454	May 09, 2011 (134)
37	ILLUMINA	ss410920383	Sep 17, 2011 (135)
38	ILLUMINA	ss480461617	May 04, 2012 (137)
39	ILLUMINA	ss480475790	May 04, 2012 (137)
40	ILLUMINA	ss481270164	Sep 08, 2015 (146)
41	ILLUMINA	ss485028275	May 04, 2012 (137)
42	ILLUMINA	ss537053563	Sep 08, 2015 (146)
43	TISHKOFF	ss566518926	Apr 25, 2013 (138)
44	SSMP	ss662429777	Apr 25, 2013 (138)
45	ILLUMINA	ss778858614	Sep 08, 2015 (146)
46	ILLUMINA	ss782960410	Sep 08, 2015 (146)
47	ILLUMINA	ss783922505	Sep 08, 2015 (146)
48	ILLUMINA	ss832216587	Sep 08, 2015 (146)
49	ILLUMINA	ss832879569	Jul 13, 2019 (153)
50	ILLUMINA	ss834319361	Sep 08, 2015 (146)
51	EVA-GONL	ss995154100	Aug 21, 2014 (142)
52	JMKIDD_LAB	ss1082527062	Aug 21, 2014 (142)
53	1000GENOMES	ss1366419976	Aug 21, 2014 (142)
54	DDI	ss1429195485	Apr 01, 2015 (144)
55	EVA_GENOME_DK	ss1579677621	Apr 01, 2015 (144)
56	EVA_UK10K_ALSPAC	ss1639633606	Apr 01, 2015 (144)
57	EVA_UK10K_ALSPAC	ss1639633607	Apr 01, 2015 (144)
58	EVA_UK10K_TWINSUK	ss1682627639	Apr 01, 2015 (144)
59	EVA_UK10K_TWINSUK	ss1682627640	Apr 01, 2015 (144)
60	EVA_DECODE	ss1699225997	Apr 01, 2015 (144)
61	EVA_DECODE	ss1699225998	Apr 01, 2015 (144)
62	EVA_SVP	ss1713726479	Apr 01, 2015 (144)
63	HAMMER_LAB	ss1809703797	Sep 08, 2015 (146)
64	WEILL_CORNELL_DGM	ss1938704426	Feb 12, 2016 (147)
65	GENOMED	ss1969233793	Jul 19, 2016 (147)
66	JJLAB	ss2030126314	Sep 14, 2016 (149)
67	USC_VALOUEV	ss2158731449	Dec 20, 2016 (150)
68	HUMAN_LONGEVITY	ss2246046528	Dec 20, 2016 (150)
69	GRF	ss2704462958	Nov 08, 2017 (151)
70	GNOMAD	ss2972158394	Nov 08, 2017 (151)
71	SWEGEN	ss3018946830	Nov 08, 2017 (151)
72	BIOINF_KMB_FNS_UNIBA	ss3028902947	Nov 08, 2017 (151)
73	CSHL	ss3352735715	Nov 08, 2017 (151)
74	ILLUMINA	ss3628489941	Oct 12, 2018 (152)
75	ILLUMINA	ss3631807372	Oct 12, 2018 (152)
76	ILLUMINA	ss3633266627	Oct 12, 2018 (152)
77	ILLUMINA	ss3633981666	Oct 12, 2018 (152)
78	ILLUMINA	ss3636552800	Oct 12, 2018 (152)
79	ILLUMINA	ss3638370212	Oct 12, 2018 (152)
80	ILLUMINA	ss3639189146	Oct 12, 2018 (152)
81	ILLUMINA	ss3639896943	Oct 12, 2018 (152)
82	ILLUMINA	ss3643331013	Oct 12, 2018 (152)
83	ILLUMINA	ss3643944386	Oct 12, 2018 (152)
84	URBANLAB	ss3651123646	Oct 12, 2018 (152)
85	EGCUT_WGS	ss3685524505	Jul 13, 2019 (153)
86	EVA_DECODE	ss3707800918	Jul 13, 2019 (153)
87	EVA_DECODE	ss3707800919	Jul 13, 2019 (153)
88	ACPOP	ss3743762845	Jul 13, 2019 (153)
89	EVA	ss3759149922	Jul 13, 2019 (153)
90	PACBIO	ss3788773342	Jul 13, 2019 (153)
91	PACBIO	ss3793646339	Jul 13, 2019 (153)
92	PACBIO	ss3798532642	Jul 13, 2019 (153)
93	KHV_HUMAN_GENOMES	ss3822316514	Jul 13, 2019 (153)
94	EVA	ss3835893227	Apr 27, 2020 (154)
95	EVA	ss3841574206	Apr 27, 2020 (154)
96	EVA	ss3847087885	Apr 27, 2020 (154)
97	HGDP	ss3847682519	Apr 27, 2020 (154)
98	SGDP_PRJ	ss3890075296	Apr 27, 2020 (154)
99	KRGDB	ss3940421052	Apr 27, 2020 (154)
100	EVA	ss3985906399	Apr 27, 2021 (155)
101	TOPMED	ss5102741404	Apr 27, 2021 (155)
102	TOMMO_GENOMICS	ss5231679667	Apr 27, 2021 (155)
103	1000G_HIGH_COVERAGE	ss5310335154	Oct 16, 2022 (156)
104	EVA	ss5440102141	Oct 16, 2022 (156)
105	HUGCELL_USP	ss5502372702	Oct 16, 2022 (156)
106	1000G_HIGH_COVERAGE	ss5617531740	Oct 16, 2022 (156)
107	SANFORD_IMAGENETICS	ss5664082045	Oct 16, 2022 (156)
108	TOMMO_GENOMICS	ss5792234758	Oct 16, 2022 (156)
109	EVA	ss5800035410	Oct 16, 2022 (156)
110	YY_MCH	ss5818473874	Oct 16, 2022 (156)
111	EVA	ss5839088432	Oct 16, 2022 (156)
112	EVA	ss5839088433	Oct 16, 2022 (156)
113	EVA	ss5853321090	Oct 16, 2022 (156)
114	EVA	ss5892492613	Oct 16, 2022 (156)
115	EVA	ss5958980894	Oct 16, 2022 (156)
116	1000Genomes	NC_000021.8 - 43439620	Oct 12, 2018 (152)
117	1000Genomes_30x	NC_000021.9 - 42019511	Oct 16, 2022 (156)
118	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 44248705 (NC_000021.8:43439619:A:A 1768/3854, NC_000021.8:43439619:A:G 2086/3854) Row 44248706 (NC_000021.8:43439619:A:A 3851/3854, NC_000021.8:43439619:A:C 3/3854)	-	Oct 12, 2018 (152)
119	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 44248705 (NC_000021.8:43439619:A:A 1768/3854, NC_000021.8:43439619:A:G 2086/3854) Row 44248706 (NC_000021.8:43439619:A:A 3851/3854, NC_000021.8:43439619:A:C 3/3854)	-	Oct 12, 2018 (152)
120	Genetic variation in the Estonian population	NC_000021.8 - 43439620	Oct 12, 2018 (152)
121	The Danish reference pan genome	NC_000021.8 - 43439620	Apr 27, 2020 (154)
122	gnomAD - Genomes Submission ignored due to conflicting rows: Row 564109692 (NC_000021.9:42019510:A:C 33/140112) Row 564109693 (NC_000021.9:42019510:A:G 62556/140064)	-	Apr 27, 2021 (155)
123	gnomAD - Genomes Submission ignored due to conflicting rows: Row 564109692 (NC_000021.9:42019510:A:C 33/140112) Row 564109693 (NC_000021.9:42019510:A:G 62556/140064)	-	Apr 27, 2021 (155)
124	Genome of the Netherlands Release 5	NC_000021.8 - 43439620	Apr 27, 2020 (154)
125	HGDP-CEPH-db Supplement 1	NC_000021.7 - 42312689	Apr 27, 2020 (154)
126	HapMap	NC_000021.9 - 42019511	Apr 27, 2020 (154)
127	KOREAN population from KRGDB	NC_000021.8 - 43439620	Apr 27, 2020 (154)
128	Northern Sweden	NC_000021.8 - 43439620	Jul 13, 2019 (153)
129	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000021.8 - 43439620	Apr 27, 2021 (155)
130	Qatari	NC_000021.8 - 43439620	Apr 27, 2020 (154)
131	SGDP_PRJ	NC_000021.8 - 43439620	Apr 27, 2020 (154)
132	Siberian	NC_000021.8 - 43439620	Apr 27, 2020 (154)
133	8.3KJPN	NC_000021.8 - 43439620	Apr 27, 2021 (155)
134	14KJPN	NC_000021.9 - 42019511	Oct 16, 2022 (156)
135	TopMed	NC_000021.9 - 42019511	Apr 27, 2021 (155)
136	UK 10K study - Twins Submission ignored due to conflicting rows: Row 44248705 (NC_000021.8:43439619:A:A 1731/3708, NC_000021.8:43439619:A:G 1977/3708) Row 44248706 (NC_000021.8:43439619:A:A 3703/3708, NC_000021.8:43439619:A:C 5/3708)	-	Oct 12, 2018 (152)
137	UK 10K study - Twins Submission ignored due to conflicting rows: Row 44248705 (NC_000021.8:43439619:A:A 1731/3708, NC_000021.8:43439619:A:G 1977/3708) Row 44248706 (NC_000021.8:43439619:A:A 3703/3708, NC_000021.8:43439619:A:C 5/3708)	-	Oct 12, 2018 (152)
138	A Vietnamese Genetic Variation Database	NC_000021.8 - 43439620	Jul 13, 2019 (153)
139	ALFA	NC_000021.9 - 42019511	Apr 27, 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)
rs854840	Jan 18, 2001 (92)
rs60454191	May 26, 2008 (130)
rs386560759	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1699225997	NC_000021.7:42312688:A:C	NC_000021.9:42019510:A:C	(self)
ss1639633607, ss1682627640, ss2972158394, ss5839088433	NC_000021.8:43439619:A:C	NC_000021.9:42019510:A:C	(self)
29398679, ss2246046528, ss3707800918	NC_000021.9:42019510:A:C	NC_000021.9:42019510:A:C	(self)
360411, ss80891191, ss91849900, ss117538460, ss160513975, ss168105418, ss204028090, ss208800959, ss212091925, ss255986803, ss292717454, ss480461617, ss1699225998, ss1713726479, ss3639189146, ss3639896943, ss3643331013, ss3643944386, ss3847682519	NC_000021.7:42312688:A:G	NC_000021.9:42019510:A:G	(self)
79944921, 31262753, 5842560, 19710996, 47598446, 17047710, 1132326, 20746348, 42092276, 11247803, 89648974, 9763949, ss228584198, ss237996467, ss244132403, ss480475790, ss481270164, ss485028275, ss537053563, ss566518926, ss662429777, ss778858614, ss782960410, ss783922505, ss832216587, ss832879569, ss834319361, ss995154100, ss1082527062, ss1366419976, ss1429195485, ss1579677621, ss1639633606, ss1682627639, ss1809703797, ss1938704426, ss1969233793, ss2030126314, ss2158731449, ss2704462958, ss2972158394, ss3018946830, ss3352735715, ss3628489941, ss3631807372, ss3633266627, ss3633981666, ss3636552800, ss3638370212, ss3685524505, ss3743762845, ss3759149922, ss3788773342, ss3793646339, ss3798532642, ss3835893227, ss3841574206, ss3890075296, ss3940421052, ss3985906399, ss5231679667, ss5440102141, ss5664082045, ss5800035410, ss5839088432, ss5958980894	NC_000021.8:43439619:A:G	NC_000021.9:42019510:A:G	(self)
105057675, 2216413, 126071862, 377850350, 29398679, ss2246046528, ss3028902947, ss3651123646, ss3707800919, ss3822316514, ss3847087885, ss5102741404, ss5310335154, ss5502372702, ss5617531740, ss5792234758, ss5818473874, ss5853321090, ss5892492613	NC_000021.9:42019510:A:G	NC_000021.9:42019510:A:G	(self)
ss286493, ss472656, ss1240583, ss1837477, ss44257734, ss67233296, ss67629079, ss68198969, ss69255191, ss70711634, ss71279003, ss75650938, ss83391143, ss96172132, ss135595779, ss138322562, ss153881068, ss159367727, ss173176207, ss410920383	NT_011515.12:434060:A:G	NC_000021.9:42019510:A:G	(self)
ss10992787	NT_030188.2:188945:A:G	NC_000021.9:42019510:A:G	(self)
ss14439556, ss16911160, ss21835691	NT_030188.3:188945:A:G	NC_000021.9:42019510:A:G	(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 rs220207

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

rs220207