rs1050747

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(T;T)	0	common in clinvar

Make rs1050747(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31355519

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs1050747
dbSNP (classic)	rs1050747
ClinGen	rs1050747
ebi	rs1050747
HLI	rs1050747
Exac	rs1050747
Gnomad	rs1050747
Varsome	rs1050747
LitVar	rs1050747
Map	rs1050747
PheGenI	rs1050747
Biobank	rs1050747
1000 genomes	rs1050747
hgdp	rs1050747
ensembl	rs1050747
geneview	rs1050747
scholar	rs1050747
google	rs1050747
pharmgkb	rs1050747
gwascentral	rs1050747
openSNP	rs1050747
23andMe	rs1050747
SNPshot	rs1050747
SNPdbe	rs1050747
MSV3d	rs1050747
GWAS Ctlg	rs1050747

GMAF

0.1781

Max Magnitude

0

ClinVar
Risk	Rs1050747(C;C)
Alt	Rs1050747(C;C)
Reference	Rs1050747(T;T)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31323296A>G
CLNSRC
CLNACC