rs1050686

Orientation

minus

Stabilized

minus

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

Make rs1050686(C;T)

Make rs1050686(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31271132

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs1050686
dbSNP (classic)	rs1050686
ClinGen	rs1050686
ebi	rs1050686
HLI	rs1050686
Exac	rs1050686
Gnomad	rs1050686
Varsome	rs1050686
LitVar	rs1050686
Map	rs1050686
PheGenI	rs1050686
Biobank	rs1050686
1000 genomes	rs1050686
hgdp	rs1050686
ensembl	rs1050686
geneview	rs1050686
scholar	rs1050686
google	rs1050686
pharmgkb	rs1050686
gwascentral	rs1050686
openSNP	rs1050686
23andMe	rs1050686
SNPshot	rs1050686
SNPdbe	rs1050686
MSV3d	rs1050686
GWAS Ctlg	rs1050686

Max Magnitude

0

ClinVar
Risk	rs1050686(A;A) rs1050686(T;T)
Alt	rs1050686(A;A) rs1050686(T;T)
Reference	Rs1050686(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31238909G>A; NC_000006.11:g.31238909G>T
CLNSRC
CLNACC