rs1131156

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1131156(C;G)

Make rs1131156(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31357118

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs1131156
dbSNP (classic)	rs1131156
ClinGen	rs1131156
ebi	rs1131156
HLI	rs1131156
Exac	rs1131156
Gnomad	rs1131156
Varsome	rs1131156
LitVar	rs1131156
Map	rs1131156
PheGenI	rs1131156
Biobank	rs1131156
1000 genomes	rs1131156
hgdp	rs1131156
ensembl	rs1131156
geneview	rs1131156
scholar	rs1131156
google	rs1131156
pharmgkb	rs1131156
gwascentral	rs1131156
openSNP	rs1131156
23andMe	rs1131156
SNPshot	rs1131156
SNPdbe	rs1131156
MSV3d	rs1131156
GWAS Ctlg	rs1131156

GMAF

0.4908

Max Magnitude

0

ClinVar
Risk	rs1131156(A;A) rs1131156(G;G)
Alt	rs1131156(A;A) rs1131156(G;G)
Reference	Rs1131156(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324895G>C; NC_000006.11:g.31324895G>T
CLNSRC
CLNACC

[PMID 18974781] Cataloging coding sequence variations in human genome databases.