Name: rs255
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.

rs255

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:19954390 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.181322 (47994/264690, TOPMED)
C=0.166838 (41243/247204, GnomAD_exome)
C=0.174851 (24497/140102, GnomAD) (+ 21 more)
C=0.170583 (20024/117386, ExAC)
C=0.16773 (8014/47778, ALFA)
C=0.22057 (6233/28258, 14KJPN)
C=0.22321 (3741/16760, 8.3KJPN)
C=0.09934 (1292/13006, GO-ESP)
C=0.2114 (1354/6404, 1000G_30x)
C=0.2065 (1034/5008, 1000G)
C=0.1404 (629/4480, Estonian)
C=0.1510 (582/3854, ALSPAC)
C=0.1502 (557/3708, TWINSUK)
C=0.2099 (615/2930, KOREAN)
C=0.2101 (397/1890, HapMap)
C=0.1943 (356/1832, Korea1K)
C=0.141 (141/998, GoNL)
C=0.115 (69/600, NorthernSweden)
C=0.169 (90/534, MGP)
C=0.153 (33/216, Qatari)
T=0.413 (81/196, SGDP_PRJ)
C=0.15 (6/40, GENOME_DK)
T=0.50 (8/16, Siberian)
C=0.50 (8/16, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: LPL : Intron Variant
Publications: 2 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	47778	T=0.83227	C=0.16773	0.694629	0.030098	0.275273	3
European	Sub	34692	T=0.84850	C=0.15150	0.7208	0.02381	0.25539	0
African	Sub	7554	T=0.7675	C=0.2325	0.590151	0.05507	0.354779	0
African Others	Sub	250	T=0.748	C=0.252	0.592	0.096	0.312	2
African American	Sub	7304	T=0.7682	C=0.2318	0.590088	0.053669	0.356243	0
Asian	Sub	192	T=0.719	C=0.281	0.5	0.0625	0.4375	0
East Asian	Sub	134	T=0.694	C=0.306	0.477612	0.089552	0.432836	0
Other Asian	Sub	58	T=0.78	C=0.22	0.551724	0.0	0.448276	2
Latin American 1	Sub	182	T=0.846	C=0.154	0.714286	0.021978	0.263736	0
Latin American 2	Sub	754	T=0.840	C=0.160	0.718833	0.039788	0.241379	3
South Asian	Sub	114	T=0.754	C=0.246	0.596491	0.087719	0.315789	1
Other	Sub	4290	T=0.8203	C=0.1797	0.673193	0.032634	0.294172	0

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.818678	C=0.181322
gnomAD - Exomes	Global	Study-wide	247204	T=0.833162	C=0.166838
gnomAD - Exomes	European	Sub	132352	T=0.860977	C=0.139023
gnomAD - Exomes	Asian	Sub	48556	T=0.77704	C=0.22296
gnomAD - Exomes	American	Sub	34202	T=0.84279	C=0.15721
gnomAD - Exomes	African	Sub	16044	T=0.76764	C=0.23236
gnomAD - Exomes	Ashkenazi Jewish	Sub	10000	T=0.8050	C=0.1950
gnomAD - Exomes	Other	Sub	6050	T=0.8410	C=0.1590
gnomAD - Genomes	Global	Study-wide	140102	T=0.825149	C=0.174851
gnomAD - Genomes	European	Sub	75908	T=0.85594	C=0.14406
gnomAD - Genomes	African	Sub	41944	T=0.77356	C=0.22644
gnomAD - Genomes	American	Sub	13644	T=0.82439	C=0.17561
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.8066	C=0.1934
gnomAD - Genomes	East Asian	Sub	3128	T=0.7868	C=0.2132
gnomAD - Genomes	Other	Sub	2154	T=0.8338	C=0.1662
ExAC	Global	Study-wide	117386	T=0.829417	C=0.170583
ExAC	Europe	Sub	71008	T=0.85492	C=0.14508
ExAC	Asian	Sub	24420	T=0.77338	C=0.22662
ExAC	American	Sub	10980	T=0.84098	C=0.15902
ExAC	African	Sub	10084	T=0.77043	C=0.22957
ExAC	Other	Sub	894	T=0.858	C=0.142
Allele Frequency Aggregator	Total	Global	47778	T=0.83227	C=0.16773
Allele Frequency Aggregator	European	Sub	34692	T=0.84850	C=0.15150
Allele Frequency Aggregator	African	Sub	7554	T=0.7675	C=0.2325
Allele Frequency Aggregator	Other	Sub	4290	T=0.8203	C=0.1797
Allele Frequency Aggregator	Latin American 2	Sub	754	T=0.840	C=0.160
Allele Frequency Aggregator	Asian	Sub	192	T=0.719	C=0.281
Allele Frequency Aggregator	Latin American 1	Sub	182	T=0.846	C=0.154
Allele Frequency Aggregator	South Asian	Sub	114	T=0.754	C=0.246
14KJPN	JAPANESE	Study-wide	28258	T=0.77943	C=0.22057
8.3KJPN	JAPANESE	Study-wide	16760	T=0.77679	C=0.22321
GO Exome Sequencing Project	Global	Study-wide	13006	T=0.90066	C=0.09934
GO Exome Sequencing Project	European American	Sub	8600	T=0.9230	C=0.0770
GO Exome Sequencing Project	African American	Sub	4406	T=0.8570	C=0.1430
1000Genomes_30x	Global	Study-wide	6404	T=0.7886	C=0.2114
1000Genomes_30x	African	Sub	1786	T=0.7738	C=0.2262
1000Genomes_30x	Europe	Sub	1266	T=0.8325	C=0.1675
1000Genomes_30x	South Asian	Sub	1202	T=0.7671	C=0.2329
1000Genomes_30x	East Asian	Sub	1170	T=0.7487	C=0.2513
1000Genomes_30x	American	Sub	980	T=0.833	C=0.167
1000Genomes	Global	Study-wide	5008	T=0.7935	C=0.2065
1000Genomes	African	Sub	1322	T=0.7814	C=0.2186
1000Genomes	East Asian	Sub	1008	T=0.7520	C=0.2480
1000Genomes	Europe	Sub	1006	T=0.8479	C=0.1521
1000Genomes	South Asian	Sub	978	T=0.764	C=0.236
1000Genomes	American	Sub	694	T=0.840	C=0.160
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8596	C=0.1404
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8490	C=0.1510
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8498	C=0.1502
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.7901	C=0.2099
HapMap	Global	Study-wide	1890	T=0.7899	C=0.2101
HapMap	American	Sub	770	T=0.803	C=0.197
HapMap	African	Sub	690	T=0.770	C=0.230
HapMap	Asian	Sub	254	T=0.776	C=0.224
HapMap	Europe	Sub	176	T=0.835	C=0.165
Korean Genome Project	KOREAN	Study-wide	1832	T=0.8057	C=0.1943
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.859	C=0.141
Northern Sweden	ACPOP	Study-wide	600	T=0.885	C=0.115
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.831	C=0.169
Qatari	Global	Study-wide	216	T=0.847	C=0.153
SGDP_PRJ	Global	Study-wide	196	T=0.413	C=0.587
The Danish reference pan genome	Danish	Study-wide	40	T=0.85	C=0.15
Siberian	Global	Study-wide	16	T=0.50	C=0.50

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 8	NC_000008.11:g.19954390T>C
GRCh37.p13 chr 8	NC_000008.10:g.19811901T>C
LPL RefSeqGene (LRG_1298)	NG_008855.2:g.57674T>C

Gene: LPL, lipoprotein lipase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LPL transcript	NM_000237.3:c.775+37T>C	N/A	Intron 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: C (allele ID: 1171839 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001540357.2	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	T=	C
GRCh38.p14 chr 8	NC_000008.11:g.19954390=	NC_000008.11:g.19954390T>C
GRCh37.p13 chr 8	NC_000008.10:g.19811901=	NC_000008.10:g.19811901T>C
LPL RefSeqGene (LRG_1298)	NG_008855.2:g.57674=	NG_008855.2:g.57674T>C
LPL transcript	NM_000237.2:c.775+37=	NM_000237.2:c.775+37T>C
LPL transcript	NM_000237.3:c.775+37=	NM_000237.3:c.775+37T>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#.

94 SubSNP, 23 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	DEBNICK	ss255	Sep 19, 2000 (36)
2	WI_SSAHASNP	ss6803993	Feb 20, 2003 (111)
3	BCM_SSAHASNP	ss10421747	Jul 11, 2003 (116)
4	ILLUMINA	ss65750586	Oct 15, 2006 (127)
5	ILLUMINA	ss74989534	Dec 07, 2007 (129)
6	BGI	ss104512504	Dec 01, 2009 (131)
7	KRIBB_YJKIM	ss119336838	Dec 01, 2009 (131)
8	COMPLETE_GENOMICS	ss162223993	Jul 04, 2010 (132)
9	ILLUMINA	ss173388011	Jul 04, 2010 (132)
10	BUSHMAN	ss198888082	Jul 04, 2010 (132)
11	1000GENOMES	ss223585621	Jul 14, 2010 (132)
12	1000GENOMES	ss234352465	Jul 15, 2010 (132)
13	1000GENOMES	ss241227289	Jul 15, 2010 (132)
14	ILLUMINA	ss244291051	Jul 04, 2010 (132)
15	BL	ss254171396	May 09, 2011 (134)
16	GMI	ss279724010	May 04, 2012 (137)
17	ILLUMINA	ss410878527	Sep 17, 2011 (135)
18	ILLUMINA	ss484373144	May 04, 2012 (137)
19	ILLUMINA	ss485584676	May 04, 2012 (137)
20	1000GENOMES	ss490960917	May 04, 2012 (137)
21	ILLUMINA	ss536555477	Sep 08, 2015 (146)
22	TISHKOFF	ss560600101	Apr 25, 2013 (138)
23	SSMP	ss655035539	Apr 25, 2013 (138)
24	NHLBI-ESP	ss712828526	Apr 25, 2013 (138)
25	ILLUMINA	ss780629202	Sep 08, 2015 (146)
26	ILLUMINA	ss782632906	Sep 08, 2015 (146)
27	ILLUMINA	ss836122976	Sep 08, 2015 (146)
28	EVA-GONL	ss985272606	Aug 21, 2014 (142)
29	JMKIDD_LAB	ss1075339991	Aug 21, 2014 (142)
30	1000GENOMES	ss1328915082	Aug 21, 2014 (142)
31	DDI	ss1431441572	Apr 01, 2015 (144)
32	EVA_GENOME_DK	ss1582593746	Apr 01, 2015 (144)
33	EVA_DECODE	ss1594862262	Apr 01, 2015 (144)
34	EVA_UK10K_ALSPAC	ss1620133675	Apr 01, 2015 (144)
35	EVA_UK10K_TWINSUK	ss1663127708	Apr 01, 2015 (144)
36	EVA_EXAC	ss1689111531	Apr 01, 2015 (144)
37	EVA_MGP	ss1711194698	Apr 01, 2015 (144)
38	EVA_SVP	ss1713021085	Apr 01, 2015 (144)
39	HAMMER_LAB	ss1805432774	Sep 08, 2015 (146)
40	WEILL_CORNELL_DGM	ss1928562354	Feb 12, 2016 (147)
41	GENOMED	ss1970929928	Jul 19, 2016 (147)
42	JJLAB	ss2024980539	Sep 14, 2016 (149)
43	USC_VALOUEV	ss2153202005	Dec 20, 2016 (150)
44	HUMAN_LONGEVITY	ss2301287827	Dec 20, 2016 (150)
45	SYSTEMSBIOZJU	ss2626975140	Nov 08, 2017 (151)
46	ILLUMINA	ss2634720439	Nov 08, 2017 (151)
47	GRF	ss2708962514	Nov 08, 2017 (151)
48	GNOMAD	ss2737022323	Nov 08, 2017 (151)
49	GNOMAD	ss2748007707	Nov 08, 2017 (151)
50	GNOMAD	ss2864092719	Nov 08, 2017 (151)
51	AFFY	ss2986076168	Nov 08, 2017 (151)
52	SWEGEN	ss3002804420	Nov 08, 2017 (151)
53	BIOINF_KMB_FNS_UNIBA	ss3026281095	Nov 08, 2017 (151)
54	CSHL	ss3348082018	Nov 08, 2017 (151)
55	ILLUMINA	ss3630013632	Oct 12, 2018 (152)
56	ILLUMINA	ss3632620990	Oct 12, 2018 (152)
57	ILLUMINA	ss3638748365	Oct 12, 2018 (152)
58	ILLUMINA	ss3642618964	Oct 12, 2018 (152)
59	ILLUMINA	ss3643680163	Oct 12, 2018 (152)
60	OMUKHERJEE_ADBS	ss3646373016	Oct 12, 2018 (152)
61	EGCUT_WGS	ss3670484445	Jul 13, 2019 (153)
62	EVA_DECODE	ss3721555421	Jul 13, 2019 (153)
63	ACPOP	ss3735467023	Jul 13, 2019 (153)
64	EVA	ss3767717741	Jul 13, 2019 (153)
65	PACBIO	ss3786087357	Jul 13, 2019 (153)
66	PACBIO	ss3791353766	Jul 13, 2019 (153)
67	PACBIO	ss3796234933	Jul 13, 2019 (153)
68	KHV_HUMAN_GENOMES	ss3810881202	Jul 13, 2019 (153)
69	EVA	ss3824351397	Apr 26, 2020 (154)
70	EVA	ss3825737072	Apr 26, 2020 (154)
71	EVA	ss3831054894	Apr 26, 2020 (154)
72	SGDP_PRJ	ss3869436688	Apr 26, 2020 (154)
73	KRGDB	ss3916862519	Apr 26, 2020 (154)
74	KOGIC	ss3963402153	Apr 26, 2020 (154)
75	FSA-LAB	ss3984393690	Apr 27, 2021 (155)
76	FSA-LAB	ss3984393691	Apr 27, 2021 (155)
77	EVA	ss3986415470	Apr 27, 2021 (155)
78	EVA	ss4017379935	Apr 27, 2021 (155)
79	TOPMED	ss4778092589	Apr 27, 2021 (155)
80	TOMMO_GENOMICS	ss5187654382	Apr 27, 2021 (155)
81	1000G_HIGH_COVERAGE	ss5276330126	Oct 14, 2022 (156)
82	EVA	ss5315316831	Oct 14, 2022 (156)
83	HUGCELL_USP	ss5472980748	Oct 14, 2022 (156)
84	EVA	ss5509275466	Oct 14, 2022 (156)
85	1000G_HIGH_COVERAGE	ss5566253965	Oct 14, 2022 (156)
86	EVA	ss5624176079	Oct 14, 2022 (156)
87	SANFORD_IMAGENETICS	ss5644923817	Oct 14, 2022 (156)
88	TOMMO_GENOMICS	ss5729270970	Oct 14, 2022 (156)
89	YY_MCH	ss5809516727	Oct 14, 2022 (156)
90	EVA	ss5830224451	Oct 14, 2022 (156)
91	EVA	ss5848702261	Oct 14, 2022 (156)
92	EVA	ss5856287085	Oct 14, 2022 (156)
93	EVA	ss5888021454	Oct 14, 2022 (156)
94	EVA	ss5974104308	Oct 14, 2022 (156)
95	1000Genomes	NC_000008.10 - 19811901	Oct 12, 2018 (152)
96	1000Genomes_30x	NC_000008.11 - 19954390	Oct 14, 2022 (156)
97	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 19811901	Oct 12, 2018 (152)
98	Genetic variation in the Estonian population	NC_000008.10 - 19811901	Oct 12, 2018 (152)
99	ExAC	NC_000008.10 - 19811901	Oct 12, 2018 (152)
100	The Danish reference pan genome	NC_000008.10 - 19811901	Apr 26, 2020 (154)
101	gnomAD - Genomes	NC_000008.11 - 19954390	Apr 27, 2021 (155)
102	gnomAD - Exomes	NC_000008.10 - 19811901	Jul 13, 2019 (153)
103	GO Exome Sequencing Project	NC_000008.10 - 19811901	Oct 12, 2018 (152)
104	Genome of the Netherlands Release 5	NC_000008.10 - 19811901	Apr 26, 2020 (154)
105	HapMap	NC_000008.11 - 19954390	Apr 26, 2020 (154)
106	KOREAN population from KRGDB	NC_000008.10 - 19811901	Apr 26, 2020 (154)
107	Korean Genome Project	NC_000008.11 - 19954390	Apr 26, 2020 (154)
108	Medical Genome Project healthy controls from Spanish population	NC_000008.10 - 19811901	Apr 26, 2020 (154)
109	Northern Sweden	NC_000008.10 - 19811901	Jul 13, 2019 (153)
110	Qatari	NC_000008.10 - 19811901	Apr 26, 2020 (154)
111	SGDP_PRJ	NC_000008.10 - 19811901	Apr 26, 2020 (154)
112	Siberian	NC_000008.10 - 19811901	Apr 26, 2020 (154)
113	8.3KJPN	NC_000008.10 - 19811901	Apr 27, 2021 (155)
114	14KJPN	NC_000008.11 - 19954390	Oct 14, 2022 (156)
115	TopMed	NC_000008.11 - 19954390	Apr 27, 2021 (155)
116	UK 10K study - Twins	NC_000008.10 - 19811901	Oct 12, 2018 (152)
117	ALFA	NC_000008.11 - 19954390	Apr 27, 2021 (155)
118	ClinVar	RCV001540357.2	Oct 14, 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
ss162223993, ss198888082, ss254171396, ss279724010, ss485584676, ss1594862262, ss1713021085, ss3643680163	NC_000008.9:19856180:T:C	NC_000008.11:19954389:T:C	(self)
41009824, 22797067, 16222693, 9205125, 8758684, 6190706, 809249, 10186922, 24039913, 310458, 8751888, 10604284, 21453668, 5718359, 45623689, 22797067, ss223585621, ss234352465, ss241227289, ss484373144, ss490960917, ss536555477, ss560600101, ss655035539, ss712828526, ss780629202, ss782632906, ss836122976, ss985272606, ss1075339991, ss1328915082, ss1431441572, ss1582593746, ss1620133675, ss1663127708, ss1689111531, ss1711194698, ss1805432774, ss1928562354, ss1970929928, ss2024980539, ss2153202005, ss2626975140, ss2634720439, ss2708962514, ss2737022323, ss2748007707, ss2864092719, ss2986076168, ss3002804420, ss3348082018, ss3630013632, ss3632620990, ss3638748365, ss3642618964, ss3646373016, ss3670484445, ss3735467023, ss3767717741, ss3786087357, ss3791353766, ss3796234933, ss3824351397, ss3825737072, ss3831054894, ss3869436688, ss3916862519, ss3984393690, ss3984393691, ss3986415470, ss4017379935, ss5187654382, ss5315316831, ss5509275466, ss5624176079, ss5644923817, ss5830224451, ss5848702261, ss5974104308	NC_000008.10:19811900:T:C	NC_000008.11:19954389:T:C	(self)
RCV001540357.2, 53779900, 289194548, 3580969, 19780154, 63108074, 615470149, 7261945919, ss2301287827, ss3026281095, ss3721555421, ss3810881202, ss3963402153, ss4778092589, ss5276330126, ss5472980748, ss5566253965, ss5729270970, ss5809516727, ss5856287085, ss5888021454	NC_000008.11:19954389:T:C	NC_000008.11:19954389:T:C	(self)
ss10421747	NT_030737.7:3533124:T:C	NC_000008.11:19954389:T:C	(self)
ss255, ss6803993, ss65750586, ss74989534, ss104512504, ss119336838, ss173388011, ss244291051, ss410878527	NT_167187.1:7670046:T:C	NC_000008.11:19954389:T:C	(self)

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

2 citations for rs255

PMID	Title	Author	Year	Journal
20410100	Genetic variation in APOJ, LPL, and TNFRSF10B affects plasma fatty acid distribution in Alaskan Eskimos.	Voruganti VS et al.	2010	The American journal of clinical nutrition
21303902	Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol.	Edmondson AC et al.	2011	Circulation. Cardiovascular genetics

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs255