rs1050486

Orientation

minus

Stabilized

minus

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

Make rs1050486(A;A)

Make rs1050486(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356925

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs1050486
dbSNP (classic)	rs1050486
ClinGen	rs1050486
ebi	rs1050486
HLI	rs1050486
Exac	rs1050486
Gnomad	rs1050486
Varsome	rs1050486
LitVar	rs1050486
Map	rs1050486
PheGenI	rs1050486
Biobank	rs1050486
1000 genomes	rs1050486
hgdp	rs1050486
ensembl	rs1050486
geneview	rs1050486
scholar	rs1050486
google	rs1050486
pharmgkb	rs1050486
gwascentral	rs1050486
openSNP	rs1050486
23andMe	rs1050486
SNPshot	rs1050486
SNPdbe	rs1050486
MSV3d	rs1050486
GWAS Ctlg	rs1050486

GMAF

0.3935

Max Magnitude

0

ClinVar
Risk	rs1050486(A;A) rs1050486(C;C)
Alt	rs1050486(A;A) rs1050486(C;C)
Reference	Rs1050486(G;G)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324702C>G; NC_000006.11:g.31324702C>T
CLNSRC
CLNACC