rs1050393

Orientation

minus

Stabilized

minus

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

Make rs1050393(A;G)

Make rs1050393(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356742

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs1050393
dbSNP (classic)	rs1050393
ClinGen	rs1050393
ebi	rs1050393
HLI	rs1050393
Exac	rs1050393
Gnomad	rs1050393
Varsome	rs1050393
LitVar	rs1050393
Map	rs1050393
PheGenI	rs1050393
Biobank	rs1050393
1000 genomes	rs1050393
hgdp	rs1050393
ensembl	rs1050393
geneview	rs1050393
scholar	rs1050393
google	rs1050393
pharmgkb	rs1050393
gwascentral	rs1050393
openSNP	rs1050393
23andMe	rs1050393
SNPshot	rs1050393
SNPdbe	rs1050393
MSV3d	rs1050393
GWAS Ctlg	rs1050393

Max Magnitude

0

ClinVar
Risk	rs1050393(G;G)
Alt	rs1050393(G;G)
Reference	Rs1050393(A;A)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324519T>C
CLNSRC
CLNACC