rs1049853

Orientation

minus

Stabilized

minus

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

Make rs1049853(C;T)

Make rs1049853(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31269123

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs1049853
dbSNP (classic)	rs1049853
ClinGen	rs1049853
ebi	rs1049853
HLI	rs1049853
Exac	rs1049853
Gnomad	rs1049853
Varsome	rs1049853
LitVar	rs1049853
Map	rs1049853
PheGenI	rs1049853
Biobank	rs1049853
1000 genomes	rs1049853
hgdp	rs1049853
ensembl	rs1049853
geneview	rs1049853
scholar	rs1049853
google	rs1049853
pharmgkb	rs1049853
gwascentral	rs1049853
openSNP	rs1049853
23andMe	rs1049853
SNPshot	rs1049853
SNPdbe	rs1049853
MSV3d	rs1049853
GWAS Ctlg	rs1049853

GMAF

0.1125

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	rs1049853(T;T)
Alt	rs1049853(T;T)
Reference	Rs1049853(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31236900G>A
CLNSRC
CLNACC