Name: rs4790230
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.

rs4790230

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:4771101 (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: T>A / T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.314217 (83170/264690, TOPMED)
T=0.252640 (45017/178186, ALFA)
T=0.26766 (7563/28256, 14KJPN) (+ 18 more)
T=0.26933 (4514/16760, 8.3KJPN)
T=0.3023 (1936/6404, 1000G_30x)
T=0.3013 (1509/5008, 1000G)
T=0.2313 (1036/4480, Estonian)
T=0.2517 (970/3854, ALSPAC)
T=0.2427 (900/3708, TWINSUK)
T=0.2758 (808/2930, KOREAN)
T=0.2893 (603/2084, HGDP_Stanford)
T=0.2647 (485/1832, Korea1K)
T=0.3201 (573/1790, HapMap)
T=0.238 (238/998, GoNL)
T=0.258 (155/600, NorthernSweden)
T=0.204 (103/504, SGDP_PRJ)
T=0.171 (37/216, Qatari)
T=0.201 (43/214, Vietnamese)
T=0.18 (16/88, Ancient Sardinia)
T=0.29 (14/48, Siberian)
T=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TM4SF5 : 2KB Upstream 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	178186	T=0.252640	A=0.000000, C=0.747360
European	Sub	152112	T=0.240264	A=0.000000, C=0.759736
African	Sub	7368	T=0.4691	A=0.0000, C=0.5309
African Others	Sub	242	T=0.455	A=0.000, C=0.545
African American	Sub	7126	T=0.4695	A=0.0000, C=0.5305
Asian	Sub	592	T=0.186	A=0.000, C=0.814
East Asian	Sub	470	T=0.204	A=0.000, C=0.796
Other Asian	Sub	122	T=0.115	A=0.000, C=0.885
Latin American 1	Sub	690	T=0.283	A=0.000, C=0.717
Latin American 2	Sub	6270	T=0.3518	A=0.0000, C=0.6482
South Asian	Sub	4946	T=0.1810	A=0.0000, C=0.8190
Other	Sub	6208	T=0.2590	A=0.0000, C=0.7410

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	T=0.314217	C=0.685783
Allele Frequency Aggregator	Total	Global	178186	T=0.252640	A=0.000000, C=0.747360
Allele Frequency Aggregator	European	Sub	152112	T=0.240264	A=0.000000, C=0.759736
Allele Frequency Aggregator	African	Sub	7368	T=0.4691	A=0.0000, C=0.5309
Allele Frequency Aggregator	Latin American 2	Sub	6270	T=0.3518	A=0.0000, C=0.6482
Allele Frequency Aggregator	Other	Sub	6208	T=0.2590	A=0.0000, C=0.7410
Allele Frequency Aggregator	South Asian	Sub	4946	T=0.1810	A=0.0000, C=0.8190
Allele Frequency Aggregator	Latin American 1	Sub	690	T=0.283	A=0.000, C=0.717
Allele Frequency Aggregator	Asian	Sub	592	T=0.186	A=0.000, C=0.814
14KJPN	JAPANESE	Study-wide	28256	T=0.26766	C=0.73234
8.3KJPN	JAPANESE	Study-wide	16760	T=0.26933	C=0.73067
1000Genomes_30x	Global	Study-wide	6404	T=0.3023	C=0.6977
1000Genomes_30x	African	Sub	1786	T=0.4910	C=0.5090
1000Genomes_30x	Europe	Sub	1266	T=0.2425	C=0.7575
1000Genomes_30x	South Asian	Sub	1202	T=0.1547	C=0.8453
1000Genomes_30x	East Asian	Sub	1170	T=0.2376	C=0.7624
1000Genomes_30x	American	Sub	980	T=0.294	C=0.706
1000Genomes	Global	Study-wide	5008	T=0.3013	C=0.6987
1000Genomes	African	Sub	1322	T=0.4955	C=0.5045
1000Genomes	East Asian	Sub	1008	T=0.2361	C=0.7639
1000Genomes	Europe	Sub	1006	T=0.2515	C=0.7485
1000Genomes	South Asian	Sub	978	T=0.160	C=0.840
1000Genomes	American	Sub	694	T=0.298	C=0.702
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.2313	C=0.7688
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.2517	C=0.7483
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.2427	C=0.7573
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.2758	A=0.0000, C=0.7242
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.2893	C=0.7107
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.234	C=0.766
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.256	C=0.744
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.191	C=0.809
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.272	C=0.728
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.521	C=0.479
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.481	C=0.519
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.04	C=0.96
Korean Genome Project	KOREAN	Study-wide	1832	T=0.2647	C=0.7353
HapMap	Global	Study-wide	1790	T=0.3201	C=0.6799
HapMap	African	Sub	690	T=0.439	C=0.561
HapMap	American	Sub	670	T=0.246	C=0.754
HapMap	Asian	Sub	254	T=0.252	C=0.748
HapMap	Europe	Sub	176	T=0.233	C=0.767
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.238	C=0.762
Northern Sweden	ACPOP	Study-wide	600	T=0.258	C=0.742
SGDP_PRJ	Global	Study-wide	504	T=0.204	C=0.796
Qatari	Global	Study-wide	216	T=0.171	C=0.829
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.201	C=0.799
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	88	T=0.18	C=0.82
Siberian	Global	Study-wide	48	T=0.29	C=0.71
The Danish reference pan genome	Danish	Study-wide	40	T=0.23	C=0.78

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 17	NC_000017.11:g.4771101T>A
GRCh38.p14 chr 17	NC_000017.11:g.4771101T>C
GRCh37.p13 chr 17	NC_000017.10:g.4674396T>A
GRCh37.p13 chr 17	NC_000017.10:g.4674396T>C

Gene: TM4SF5, transmembrane 4 L six family member 5 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TM4SF5 transcript	NM_003963.3:c.	N/A	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	T=	A	C
GRCh38.p14 chr 17	NC_000017.11:g.4771101=	NC_000017.11:g.4771101T>A	NC_000017.11:g.4771101T>C
GRCh37.p13 chr 17	NC_000017.10:g.4674396=	NC_000017.10:g.4674396T>A	NC_000017.10:g.4674396T>C

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#.

121 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss6610326	Feb 20, 2003 (111)
2	PERLEGEN	ss23792817	Sep 20, 2004 (123)
3	ABI	ss28532902	Dec 02, 2004 (126)
4	ILLUMINA	ss67377069	Nov 29, 2006 (127)
5	ILLUMINA	ss67756969	Nov 29, 2006 (127)
6	ILLUMINA	ss68236657	Dec 12, 2006 (127)
7	PERLEGEN	ss69189792	May 16, 2007 (127)
8	ILLUMINA	ss70825181	May 23, 2008 (130)
9	ILLUMINA	ss71407206	May 16, 2007 (127)
10	ILLUMINA	ss75656294	Dec 07, 2007 (129)
11	HGSV	ss81717483	Dec 14, 2007 (130)
12	KRIBB_YJKIM	ss84353852	Dec 14, 2007 (130)
13	BCMHGSC_JDW	ss90516455	Mar 24, 2008 (129)
14	HUMANGENOME_JCVI	ss96531796	Feb 03, 2009 (130)
15	BGI	ss103327351	Feb 23, 2009 (131)
16	1000GENOMES	ss109607772	Jan 24, 2009 (130)
17	1000GENOMES	ss113229119	Jan 25, 2009 (130)
18	ILLUMINA-UK	ss117982353	Feb 14, 2009 (130)
19	ENSEMBL	ss136950767	Dec 01, 2009 (131)
20	ENSEMBL	ss143460219	Dec 01, 2009 (131)
21	ILLUMINA	ss154317565	Dec 01, 2009 (131)
22	GMI	ss157783351	Dec 01, 2009 (131)
23	ILLUMINA	ss159494248	Dec 01, 2009 (131)
24	ILLUMINA	ss160712109	Dec 01, 2009 (131)
25	COMPLETE_GENOMICS	ss167701009	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss168946458	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss171098475	Jul 04, 2010 (132)
28	ILLUMINA	ss173814533	Jul 04, 2010 (132)
29	BCM-HGSC-SUB	ss207781252	Jul 04, 2010 (132)
30	1000GENOMES	ss227438340	Jul 14, 2010 (132)
31	1000GENOMES	ss237165115	Jul 15, 2010 (132)
32	1000GENOMES	ss243478511	Jul 15, 2010 (132)
33	BL	ss255454072	May 09, 2011 (134)
34	GMI	ss282673213	May 04, 2012 (137)
35	GMI	ss287138708	Apr 25, 2013 (138)
36	PJP	ss291962882	May 09, 2011 (134)
37	ILLUMINA	ss481049162	May 04, 2012 (137)
38	ILLUMINA	ss481070617	May 04, 2012 (137)
39	ILLUMINA	ss482062669	Sep 08, 2015 (146)
40	ILLUMINA	ss485319557	May 04, 2012 (137)
41	ILLUMINA	ss537274646	Sep 08, 2015 (146)
42	TISHKOFF	ss565137887	Apr 25, 2013 (138)
43	SSMP	ss660924689	Apr 25, 2013 (138)
44	ILLUMINA	ss778547342	Sep 08, 2015 (146)
45	ILLUMINA	ss783105598	Sep 08, 2015 (146)
46	ILLUMINA	ss784062735	Sep 08, 2015 (146)
47	ILLUMINA	ss832364210	Sep 08, 2015 (146)
48	ILLUMINA	ss833005633	Jul 13, 2019 (153)
49	ILLUMINA	ss834004030	Sep 08, 2015 (146)
50	EVA-GONL	ss992875076	Aug 21, 2014 (142)
51	JMKIDD_LAB	ss1080898013	Aug 21, 2014 (142)
52	1000GENOMES	ss1357724999	Aug 21, 2014 (142)
53	DDI	ss1427962451	Apr 01, 2015 (144)
54	EVA_GENOME_DK	ss1578069048	Apr 01, 2015 (144)
55	EVA_UK10K_ALSPAC	ss1635194139	Apr 01, 2015 (144)
56	EVA_UK10K_TWINSUK	ss1678188172	Apr 01, 2015 (144)
57	EVA_DECODE	ss1696915604	Apr 01, 2015 (144)
58	EVA_SVP	ss1713566431	Apr 01, 2015 (144)
59	ILLUMINA	ss1752228519	Sep 08, 2015 (146)
60	HAMMER_LAB	ss1808681808	Sep 08, 2015 (146)
61	WEILL_CORNELL_DGM	ss1936321508	Feb 12, 2016 (147)
62	GENOMED	ss1968341710	Jul 19, 2016 (147)
63	JJLAB	ss2028948698	Sep 14, 2016 (149)
64	USC_VALOUEV	ss2157394393	Dec 20, 2016 (150)
65	HUMAN_LONGEVITY	ss2215142611	Dec 20, 2016 (150)
66	SYSTEMSBIOZJU	ss2628965292	Nov 08, 2017 (151)
67	ILLUMINA	ss2633368935	Nov 08, 2017 (151)
68	GRF	ss2701935906	Nov 08, 2017 (151)
69	GNOMAD	ss2947184667	Nov 08, 2017 (151)
70	SWEGEN	ss3015118602	Nov 08, 2017 (151)
71	BIOINF_KMB_FNS_UNIBA	ss3028292808	Nov 08, 2017 (151)
72	CSHL	ss3351630373	Nov 08, 2017 (151)
73	ILLUMINA	ss3627613366	Oct 12, 2018 (152)
74	ILLUMINA	ss3631351805	Oct 12, 2018 (152)
75	ILLUMINA	ss3633133507	Oct 12, 2018 (152)
76	ILLUMINA	ss3633840507	Oct 12, 2018 (152)
77	ILLUMINA	ss3634661404	Oct 12, 2018 (152)
78	ILLUMINA	ss3635528496	Oct 12, 2018 (152)
79	ILLUMINA	ss3636352233	Oct 12, 2018 (152)
80	ILLUMINA	ss3637279994	Oct 12, 2018 (152)
81	ILLUMINA	ss3638146442	Oct 12, 2018 (152)
82	ILLUMINA	ss3639084203	Oct 12, 2018 (152)
83	ILLUMINA	ss3639850877	Oct 12, 2018 (152)
84	ILLUMINA	ss3640368723	Oct 12, 2018 (152)
85	ILLUMINA	ss3643126046	Oct 12, 2018 (152)
86	ILLUMINA	ss3643900436	Oct 12, 2018 (152)
87	URBANLAB	ss3650593010	Oct 12, 2018 (152)
88	EGCUT_WGS	ss3682085728	Jul 13, 2019 (153)
89	EVA_DECODE	ss3699992138	Jul 13, 2019 (153)
90	ACPOP	ss3741831458	Jul 13, 2019 (153)
91	ILLUMINA	ss3744961756	Jul 13, 2019 (153)
92	EVA	ss3754393916	Jul 13, 2019 (153)
93	ILLUMINA	ss3772459835	Jul 13, 2019 (153)
94	PACBIO	ss3788136492	Jul 13, 2019 (153)
95	PACBIO	ss3793106677	Jul 13, 2019 (153)
96	PACBIO	ss3797992264	Jul 13, 2019 (153)
97	KHV_HUMAN_GENOMES	ss3819663566	Jul 13, 2019 (153)
98	EVA	ss3834754477	Apr 27, 2020 (154)
99	EVA	ss3840985545	Apr 27, 2020 (154)
100	EVA	ss3846479791	Apr 27, 2020 (154)
101	HGDP	ss3847557227	Apr 27, 2020 (154)
102	SGDP_PRJ	ss3885241466	Apr 27, 2020 (154)
103	KRGDB	ss3934825694	Apr 27, 2020 (154)
104	KOGIC	ss3978303329	Apr 27, 2020 (154)
105	EVA	ss3985778355	Apr 26, 2021 (155)
106	TOPMED	ss5027930280	Apr 26, 2021 (155)
107	TOMMO_GENOMICS	ss5221281719	Apr 26, 2021 (155)
108	1000G_HIGH_COVERAGE	ss5302264019	Oct 17, 2022 (156)
109	EVA	ss5315869584	Oct 17, 2022 (156)
110	EVA	ss5426098407	Oct 17, 2022 (156)
111	HUGCELL_USP	ss5495456165	Oct 17, 2022 (156)
112	EVA	ss5511712643	Oct 17, 2022 (156)
113	1000G_HIGH_COVERAGE	ss5605545522	Oct 17, 2022 (156)
114	SANFORD_IMAGENETICS	ss5659632031	Oct 17, 2022 (156)
115	TOMMO_GENOMICS	ss5776811839	Oct 17, 2022 (156)
116	EVA	ss5799968965	Oct 17, 2022 (156)
117	YY_MCH	ss5816294859	Oct 17, 2022 (156)
118	EVA	ss5833657054	Oct 17, 2022 (156)
119	EVA	ss5851718814	Oct 17, 2022 (156)
120	EVA	ss5913045774	Oct 17, 2022 (156)
121	EVA	ss5951041039	Oct 17, 2022 (156)
122	1000Genomes	NC_000017.10 - 4674396	Oct 12, 2018 (152)
123	1000Genomes_30x	NC_000017.11 - 4771101	Oct 17, 2022 (156)
124	The Avon Longitudinal Study of Parents and Children	NC_000017.10 - 4674396	Oct 12, 2018 (152)
125	Genetic variation in the Estonian population	NC_000017.10 - 4674396	Oct 12, 2018 (152)
126	The Danish reference pan genome	NC_000017.10 - 4674396	Apr 27, 2020 (154)
127	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500182863 (NC_000017.11:4771100:T:A 1/140150) Row 500182864 (NC_000017.11:4771100:T:C 97418/140098)	-	Apr 26, 2021 (155)
128	gnomAD - Genomes Submission ignored due to conflicting rows: Row 500182863 (NC_000017.11:4771100:T:A 1/140150) Row 500182864 (NC_000017.11:4771100:T:C 97418/140098)	-	Apr 26, 2021 (155)
129	Genome of the Netherlands Release 5	NC_000017.10 - 4674396	Apr 27, 2020 (154)
130	HGDP-CEPH-db Supplement 1	NC_000017.9 - 4621145	Apr 27, 2020 (154)
131	HapMap	NC_000017.11 - 4771101	Apr 27, 2020 (154)
132	KOREAN population from KRGDB	NC_000017.10 - 4674396	Apr 27, 2020 (154)
133	Korean Genome Project	NC_000017.11 - 4771101	Apr 27, 2020 (154)
134	Northern Sweden	NC_000017.10 - 4674396	Jul 13, 2019 (153)
135	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000017.10 - 4674396	Apr 26, 2021 (155)
136	Qatari	NC_000017.10 - 4674396	Apr 27, 2020 (154)
137	SGDP_PRJ	NC_000017.10 - 4674396	Apr 27, 2020 (154)
138	Siberian	NC_000017.10 - 4674396	Apr 27, 2020 (154)
139	8.3KJPN	NC_000017.10 - 4674396	Apr 26, 2021 (155)
140	14KJPN	NC_000017.11 - 4771101	Oct 17, 2022 (156)
141	TopMed	NC_000017.11 - 4771101	Apr 26, 2021 (155)
142	UK 10K study - Twins	NC_000017.10 - 4674396	Oct 12, 2018 (152)
143	A Vietnamese Genetic Variation Database	NC_000017.10 - 4674396	Jul 13, 2019 (153)
144	ALFA	NC_000017.11 - 4771101	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)
rs17879391	Mar 10, 2006 (126)
rs56757274	May 23, 2008 (130)
rs74251394	Dec 02, 2009 (131)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
42003088, ss3934825694	NC_000017.10:4674395:T:A	NC_000017.11:4771100:T:A	(self)
13682743282	NC_000017.11:4771100:T:A	NC_000017.11:4771100:T:A	(self)
235119, ss81717483, ss90516455, ss109607772, ss113229119, ss117982353, ss167701009, ss168946458, ss171098475, ss207781252, ss255454072, ss282673213, ss287138708, ss291962882, ss481049162, ss1696915604, ss1713566431, ss3639084203, ss3639850877, ss3643126046, ss3643900436, ss3847557227	NC_000017.9:4621144:T:C	NC_000017.11:4771100:T:C	(self)
70932219, 39339312, 27823976, 4274889, 17538288, 42003088, 15116323, 1004282, 18363430, 37258446, 9910747, 79251026, 39339312, 8715066, ss227438340, ss237165115, ss243478511, ss481070617, ss482062669, ss485319557, ss537274646, ss565137887, ss660924689, ss778547342, ss783105598, ss784062735, ss832364210, ss833005633, ss834004030, ss992875076, ss1080898013, ss1357724999, ss1427962451, ss1578069048, ss1635194139, ss1678188172, ss1752228519, ss1808681808, ss1936321508, ss1968341710, ss2028948698, ss2157394393, ss2628965292, ss2633368935, ss2701935906, ss2947184667, ss3015118602, ss3351630373, ss3627613366, ss3631351805, ss3633133507, ss3633840507, ss3634661404, ss3635528496, ss3636352233, ss3637279994, ss3638146442, ss3640368723, ss3682085728, ss3741831458, ss3744961756, ss3754393916, ss3772459835, ss3788136492, ss3793106677, ss3797992264, ss3834754477, ss3840985545, ss3885241466, ss3934825694, ss3985778355, ss5221281719, ss5315869584, ss5426098407, ss5511712643, ss5659632031, ss5799968965, ss5833657054, ss5951041039	NC_000017.10:4674395:T:C	NC_000017.11:4771100:T:C	(self)
93071457, 1449303, 34681330, 110648943, 243475942, 13682743282, ss2215142611, ss3028292808, ss3650593010, ss3699992138, ss3819663566, ss3846479791, ss3978303329, ss5027930280, ss5302264019, ss5495456165, ss5605545522, ss5776811839, ss5816294859, ss5851718814, ss5913045774	NC_000017.11:4771100:T:C	NC_000017.11:4771100:T:C	(self)
ss6610326, ss23792817, ss28532902, ss67377069, ss67756969, ss68236657, ss69189792, ss70825181, ss71407206, ss75656294, ss84353852, ss96531796, ss103327351, ss136950767, ss143460219, ss154317565, ss157783351, ss159494248, ss160712109, ss173814533	NT_010718.16:4277769:T:C	NC_000017.11:4771100:T:C	(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 rs4790230

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

rs4790230