Name: rs10483093
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.

rs10483093

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:17492193 (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>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.166806 (44966/269570, ALFA)
G=0.132098 (34965/264690, TOPMED)
G=0.135200 (18942/140104, GnomAD) (+ 14 more)
G=0.0803 (514/6404, 1000G_30x)
G=0.0833 (417/5008, 1000G)
G=0.1625 (728/4480, Estonian)
G=0.1648 (635/3854, ALSPAC)
G=0.1826 (677/3708, TWINSUK)
G=0.0696 (145/2084, HGDP_Stanford)
G=0.0769 (126/1638, HapMap)
G=0.185 (185/998, GoNL)
G=0.008 (6/790, PRJEB37584)
G=0.190 (114/600, NorthernSweden)
G=0.074 (16/216, Qatari)
A=0.47 (33/70, SGDP_PRJ)
G=0.20 (12/60, Ancient Sardinia)
G=0.15 (6/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CECR2 : 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	274606	A=0.833460	G=0.166540
European	Sub	247540	A=0.824812	G=0.175188
African	Sub	7520	A=0.9285	G=0.0715
African Others	Sub	306	A=0.944	G=0.056
African American	Sub	7214	A=0.9278	G=0.0722
Asian	Sub	3574	A=0.9994	G=0.0006
East Asian	Sub	2868	A=0.9993	G=0.0007
Other Asian	Sub	706	A=1.000	G=0.000
Latin American 1	Sub	706	A=0.851	G=0.149
Latin American 2	Sub	2912	A=0.8444	G=0.1556
South Asian	Sub	5154	A=0.9267	G=0.0733
Other	Sub	7200	A=0.8762	G=0.1237

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
Allele Frequency Aggregator	Total	Global	269570	A=0.833194	G=0.166806
Allele Frequency Aggregator	European	Sub	244446	A=0.824967	G=0.175033
Allele Frequency Aggregator	Other	Sub	6400	A=0.8797	G=0.1203
Allele Frequency Aggregator	African	Sub	6378	A=0.9260	G=0.0740
Allele Frequency Aggregator	South Asian	Sub	5154	A=0.9267	G=0.0733
Allele Frequency Aggregator	Asian	Sub	3574	A=0.9994	G=0.0006
Allele Frequency Aggregator	Latin American 2	Sub	2912	A=0.8444	G=0.1556
Allele Frequency Aggregator	Latin American 1	Sub	706	A=0.851	G=0.149
TopMed	Global	Study-wide	264690	A=0.867902	G=0.132098
gnomAD - Genomes	Global	Study-wide	140104	A=0.864800	G=0.135200
gnomAD - Genomes	European	Sub	75878	A=0.82800	G=0.17200
gnomAD - Genomes	African	Sub	41990	A=0.92996	G=0.07004
gnomAD - Genomes	American	Sub	13634	A=0.84326	G=0.15674
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	A=0.8387	G=0.1613
gnomAD - Genomes	East Asian	Sub	3128	A=0.9997	G=0.0003
gnomAD - Genomes	Other	Sub	2150	A=0.8716	G=0.1284
1000Genomes_30x	Global	Study-wide	6404	A=0.9197	G=0.0803
1000Genomes_30x	African	Sub	1786	A=0.9513	G=0.0487
1000Genomes_30x	Europe	Sub	1266	A=0.8444	G=0.1556
1000Genomes_30x	South Asian	Sub	1202	A=0.9210	G=0.0790
1000Genomes_30x	East Asian	Sub	1170	A=0.9991	G=0.0009
1000Genomes_30x	American	Sub	980	A=0.863	G=0.137
1000Genomes	Global	Study-wide	5008	A=0.9167	G=0.0833
1000Genomes	African	Sub	1322	A=0.9493	G=0.0507
1000Genomes	East Asian	Sub	1008	A=0.9990	G=0.0010
1000Genomes	Europe	Sub	1006	A=0.8400	G=0.1600
1000Genomes	South Asian	Sub	978	A=0.918	G=0.082
1000Genomes	American	Sub	694	A=0.844	G=0.156
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.8375	G=0.1625
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.8352	G=0.1648
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.8174	G=0.1826
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.9304	G=0.0696
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.998	G=0.002
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.879	G=0.121
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.920	G=0.080
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.850	G=0.150
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.971	G=0.029
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.949	G=0.051
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=1.00	G=0.00
HapMap	Global	Study-wide	1638	A=0.9231	G=0.0769
HapMap	African	Sub	690	A=0.958	G=0.042
HapMap	American	Sub	600	A=0.892	G=0.108
HapMap	Europe	Sub	176	A=0.818	G=0.182
HapMap	Asian	Sub	172	A=1.000	G=0.000
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.815	G=0.185
CNV burdens in cranial meningiomas	Global	Study-wide	790	A=0.992	G=0.008
CNV burdens in cranial meningiomas	CRM	Sub	790	A=0.992	G=0.008
Northern Sweden	ACPOP	Study-wide	600	A=0.810	G=0.190
Qatari	Global	Study-wide	216	A=0.926	G=0.074
SGDP_PRJ	Global	Study-wide	70	A=0.47	G=0.53
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	60	A=0.80	G=0.20
The Danish reference pan genome	Danish	Study-wide	40	A=0.85	G=0.15

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 22	NC_000022.11:g.17492193A>G
GRCh37.p13 chr 22	NC_000022.10:g.17971225A>G
CECR2 RefSeqGene	NG_033989.1:g.137245A>G

Gene: CECR2, CECR2 histone acetyl-lysine reader (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CECR2 transcript variant 2	NM_001290046.2:c.-268-521… NM_001290046.2:c.-268-5210A>G	N/A	Intron Variant
CECR2 transcript variant 1	NM_001290047.2:c.222-5210… NM_001290047.2:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X2	XM_011546128.3:c.222-5210… XM_011546128.3:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X3	XM_011546129.3:c.222-5210… XM_011546129.3:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X5	XM_011546132.3:c.222-5210… XM_011546132.3:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X1	XM_017028785.2:c.222-5210… XM_017028785.2:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X4	XM_024452234.2:c.108-5210… XM_024452234.2:c.108-5210A>G	N/A	Intron Variant
CECR2 transcript variant X6	XM_047441341.1:c.222-5210… XM_047441341.1:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X7	XM_047441342.1:c.222-5210… XM_047441342.1:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X8	XM_047441343.1:c.222-5210… XM_047441343.1:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X9	XM_047441344.1:c.108-5210… XM_047441344.1:c.108-5210A>G	N/A	Intron Variant
CECR2 transcript variant X11	XM_047441345.1:c.222-5210… XM_047441345.1:c.222-5210A>G	N/A	Intron Variant
CECR2 transcript variant X10	XM_006724079.4: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	A=	G
GRCh38.p14 chr 22	NC_000022.11:g.17492193=	NC_000022.11:g.17492193A>G
GRCh37.p13 chr 22	NC_000022.10:g.17971225=	NC_000022.10:g.17971225A>G
CECR2 RefSeqGene	NG_033989.1:g.137245=	NG_033989.1:g.137245A>G
CECR2 transcript variant 2	NM_001290046.2:c.-268-5210=	NM_001290046.2:c.-268-5210A>G
CECR2 transcript variant 1	NM_001290047.2:c.222-5210=	NM_001290047.2:c.222-5210A>G
CECR2 transcript	NM_031413.3:c.96-5210=	NM_031413.3:c.96-5210A>G
CECR2 transcript variant X2	XM_011546128.3:c.222-5210=	XM_011546128.3:c.222-5210A>G
CECR2 transcript variant X3	XM_011546129.3:c.222-5210=	XM_011546129.3:c.222-5210A>G
CECR2 transcript variant X5	XM_011546132.3:c.222-5210=	XM_011546132.3:c.222-5210A>G
CECR2 transcript variant X1	XM_017028785.2:c.222-5210=	XM_017028785.2:c.222-5210A>G
CECR2 transcript variant X4	XM_024452234.2:c.108-5210=	XM_024452234.2:c.108-5210A>G
CECR2 transcript variant X6	XM_047441341.1:c.222-5210=	XM_047441341.1:c.222-5210A>G
CECR2 transcript variant X7	XM_047441342.1:c.222-5210=	XM_047441342.1:c.222-5210A>G
CECR2 transcript variant X8	XM_047441343.1:c.222-5210=	XM_047441343.1:c.222-5210A>G
CECR2 transcript variant X9	XM_047441344.1:c.108-5210=	XM_047441344.1:c.108-5210A>G
CECR2 transcript variant X11	XM_047441345.1:c.222-5210=	XM_047441345.1:c.222-5210A>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#.

96 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss14867077	Dec 05, 2003 (119)
2	PERLEGEN	ss23787211	Sep 20, 2004 (123)
3	AFFY	ss66008548	Nov 29, 2006 (127)
4	ILLUMINA	ss66569894	Nov 29, 2006 (127)
5	ILLUMINA	ss66884938	Nov 29, 2006 (127)
6	ILLUMINA	ss66981580	Nov 29, 2006 (127)
7	CSHL-HAPMAP	ss68423257	Jan 12, 2007 (127)
8	ILLUMINA	ss70366598	May 16, 2007 (127)
9	ILLUMINA	ss70480713	May 24, 2008 (130)
10	ILLUMINA	ss71004490	May 16, 2007 (127)
11	ILLUMINA	ss74935876	Dec 07, 2007 (129)
12	KRIBB_YJKIM	ss84943026	Dec 14, 2007 (130)
13	ILLUMINA	ss121311267	Dec 01, 2009 (131)
14	ILLUMINA	ss152736157	Dec 01, 2009 (131)
15	ILLUMINA	ss159125594	Dec 01, 2009 (131)
16	ILLUMINA	ss169402956	Jul 04, 2010 (132)
17	ILLUMINA	ss170140539	Jul 04, 2010 (132)
18	1000GENOMES	ss212100041	Jul 14, 2010 (132)
19	1000GENOMES	ss228610975	Jul 14, 2010 (132)
20	1000GENOMES	ss238016895	Jul 15, 2010 (132)
21	ILLUMINA	ss479279048	May 04, 2012 (137)
22	ILLUMINA	ss479282044	May 04, 2012 (137)
23	ILLUMINA	ss484440069	May 04, 2012 (137)
24	ILLUMINA	ss536609208	Sep 08, 2015 (146)
25	TISHKOFF	ss566550906	Apr 25, 2013 (138)
26	ILLUMINA	ss778732648	Sep 08, 2015 (146)
27	ILLUMINA	ss782666520	Sep 08, 2015 (146)
28	ILLUMINA	ss783635299	Sep 08, 2015 (146)
29	ILLUMINA	ss825336329	Apr 01, 2015 (144)
30	ILLUMINA	ss831917122	Sep 08, 2015 (146)
31	ILLUMINA	ss832638300	Jul 13, 2019 (153)
32	ILLUMINA	ss834192158	Sep 08, 2015 (146)
33	EVA-GONL	ss995207062	Aug 21, 2014 (142)
34	JMKIDD_LAB	ss1082560049	Aug 21, 2014 (142)
35	1000GENOMES	ss1366624579	Aug 21, 2014 (142)
36	DDI	ss1429214547	Apr 01, 2015 (144)
37	EVA_GENOME_DK	ss1579698111	Apr 01, 2015 (144)
38	EVA_UK10K_ALSPAC	ss1639726355	Apr 01, 2015 (144)
39	EVA_UK10K_TWINSUK	ss1682720388	Apr 01, 2015 (144)
40	EVA_DECODE	ss1699276561	Apr 01, 2015 (144)
41	EVA_SVP	ss1713730061	Apr 01, 2015 (144)
42	ILLUMINA	ss1752413009	Sep 08, 2015 (146)
43	WEILL_CORNELL_DGM	ss1938766303	Feb 12, 2016 (147)
44	ILLUMINA	ss1946575796	Feb 12, 2016 (147)
45	GENOMED	ss1969243969	Jul 19, 2016 (147)
46	JJLAB	ss2030156442	Sep 14, 2016 (149)
47	HUMAN_LONGEVITY	ss2246351807	Dec 20, 2016 (150)
48	ILLUMINA	ss2633860876	Nov 08, 2017 (151)
49	ILLUMINA	ss2710952511	Nov 08, 2017 (151)
50	GNOMAD	ss2972803568	Nov 08, 2017 (151)
51	SWEGEN	ss3019054925	Nov 08, 2017 (151)
52	ILLUMINA	ss3022169881	Nov 08, 2017 (151)
53	BIOINF_KMB_FNS_UNIBA	ss3028916501	Nov 08, 2017 (151)
54	CSHL	ss3352767458	Nov 08, 2017 (151)
55	ILLUMINA	ss3625799191	Oct 12, 2018 (152)
56	ILLUMINA	ss3628502404	Oct 12, 2018 (152)
57	ILLUMINA	ss3631813418	Oct 12, 2018 (152)
58	ILLUMINA	ss3633268338	Oct 12, 2018 (152)
59	ILLUMINA	ss3633983650	Oct 12, 2018 (152)
60	ILLUMINA	ss3634859971	Oct 12, 2018 (152)
61	ILLUMINA	ss3635668304	Oct 12, 2018 (152)
62	ILLUMINA	ss3637420491	Oct 12, 2018 (152)
63	ILLUMINA	ss3638373371	Oct 12, 2018 (152)
64	ILLUMINA	ss3639190625	Oct 12, 2018 (152)
65	ILLUMINA	ss3639611382	Oct 12, 2018 (152)
66	ILLUMINA	ss3640567271	Oct 12, 2018 (152)
67	ILLUMINA	ss3643333857	Oct 12, 2018 (152)
68	ILLUMINA	ss3644795710	Oct 12, 2018 (152)
69	ILLUMINA	ss3652631353	Oct 12, 2018 (152)
70	EGCUT_WGS	ss3685596526	Jul 13, 2019 (153)
71	EVA_DECODE	ss3707924152	Jul 13, 2019 (153)
72	ILLUMINA	ss3725955937	Jul 13, 2019 (153)
73	ACPOP	ss3743809203	Jul 13, 2019 (153)
74	ILLUMINA	ss3744204787	Jul 13, 2019 (153)
75	ILLUMINA	ss3745159804	Jul 13, 2019 (153)
76	EVA	ss3759212215	Jul 13, 2019 (153)
77	ILLUMINA	ss3772655799	Jul 13, 2019 (153)
78	KHV_HUMAN_GENOMES	ss3822379525	Jul 13, 2019 (153)
79	EVA	ss3835919798	Apr 27, 2020 (154)
80	HGDP	ss3847684199	Apr 27, 2020 (154)
81	SGDP_PRJ	ss3890216706	Apr 27, 2020 (154)
82	EVA	ss3984758029	Apr 27, 2021 (155)
83	EVA	ss3985909263	Apr 27, 2021 (155)
84	EVA	ss4017872750	Apr 27, 2021 (155)
85	TOPMED	ss5104635002	Apr 27, 2021 (155)
86	1000G_HIGH_COVERAGE	ss5310604432	Oct 16, 2022 (156)
87	EVA	ss5316045704	Oct 16, 2022 (156)
88	EVA	ss5440429865	Oct 16, 2022 (156)
89	HUGCELL_USP	ss5502524655	Oct 16, 2022 (156)
90	EVA	ss5512345011	Oct 16, 2022 (156)
91	1000G_HIGH_COVERAGE	ss5617936735	Oct 16, 2022 (156)
92	SANFORD_IMAGENETICS	ss5664201156	Oct 16, 2022 (156)
93	EVA	ss5821878302	Oct 16, 2022 (156)
94	EVA	ss5847938505	Oct 16, 2022 (156)
95	EVA	ss5881294126	Oct 16, 2022 (156)
96	EVA	ss5959079044	Oct 16, 2022 (156)
97	1000Genomes	NC_000022.10 - 17971225	Oct 12, 2018 (152)
98	1000Genomes_30x	NC_000022.11 - 17492193	Oct 16, 2022 (156)
99	The Avon Longitudinal Study of Parents and Children	NC_000022.10 - 17971225	Oct 12, 2018 (152)
100	Genetic variation in the Estonian population	NC_000022.10 - 17971225	Oct 12, 2018 (152)
101	The Danish reference pan genome	NC_000022.10 - 17971225	Apr 27, 2020 (154)
102	gnomAD - Genomes	NC_000022.11 - 17492193	Apr 27, 2021 (155)
103	Genome of the Netherlands Release 5	NC_000022.10 - 17971225	Apr 27, 2020 (154)
104	HGDP-CEPH-db Supplement 1	NC_000022.9 - 16351225	Apr 27, 2020 (154)
105	HapMap	NC_000022.11 - 17492193	Apr 27, 2020 (154)
106	Northern Sweden	NC_000022.10 - 17971225	Jul 13, 2019 (153)
107	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000022.10 - 17971225	Apr 27, 2021 (155)
108	CNV burdens in cranial meningiomas	NC_000022.10 - 17971225	Apr 27, 2021 (155)
109	Qatari	NC_000022.10 - 17971225	Apr 27, 2020 (154)
110	SGDP_PRJ	NC_000022.10 - 17971225	Apr 27, 2020 (154)
111	TopMed	NC_000022.11 - 17492193	Apr 27, 2021 (155)
112	UK 10K study - Twins	NC_000022.10 - 17971225	Oct 12, 2018 (152)
113	ALFA	NC_000022.11 - 17492193	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)
rs57703982	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3639190625, ss3639611382	NC_000022.8:16345778:A:G	NC_000022.11:17492192:A:G	(self)
362091, ss212100041, ss479279048, ss825336329, ss1699276561, ss1713730061, ss3643333857, ss3847684199	NC_000022.9:16351224:A:G	NC_000022.11:17492192:A:G	(self)
80156862, 44351458, 31334774, 5863050, 19759353, 17094068, 1135190, 307609, 20808225, 42233686, 44351458, ss228610975, ss238016895, ss479282044, ss484440069, ss536609208, ss566550906, ss778732648, ss782666520, ss783635299, ss831917122, ss832638300, ss834192158, ss995207062, ss1082560049, ss1366624579, ss1429214547, ss1579698111, ss1639726355, ss1682720388, ss1752413009, ss1938766303, ss1946575796, ss1969243969, ss2030156442, ss2633860876, ss2710952511, ss2972803568, ss3019054925, ss3022169881, ss3352767458, ss3625799191, ss3628502404, ss3631813418, ss3633268338, ss3633983650, ss3634859971, ss3635668304, ss3637420491, ss3638373371, ss3640567271, ss3644795710, ss3652631353, ss3685596526, ss3743809203, ss3744204787, ss3745159804, ss3759212215, ss3772655799, ss3835919798, ss3890216706, ss3984758029, ss3985909263, ss4017872750, ss5316045704, ss5440429865, ss5512345011, ss5664201156, ss5821878302, ss5847938505, ss5959079044	NC_000022.10:17971224:A:G	NC_000022.11:17492192:A:G	(self)
105462670, 566109413, 2225010, 379743949, 3350641617, ss2246351807, ss3028916501, ss3707924152, ss3725955937, ss3822379525, ss5104635002, ss5310604432, ss5502524655, ss5617936735, ss5881294126	NC_000022.11:17492192:A:G	NC_000022.11:17492192:A:G	(self)
ss14867077, ss23787211, ss66008548, ss66569894, ss66884938, ss66981580, ss68423257, ss70366598, ss70480713, ss71004490, ss74935876, ss84943026, ss121311267, ss152736157, ss159125594, ss169402956, ss170140539	NT_011519.10:1123374:A:G	NC_000022.11:17492192: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 rs10483093

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

rs10483093