rs1049663

Orientation

minus

Stabilized

minus

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

Make rs1049663(G;T)

Make rs1049663(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31269036

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs1049663
dbSNP (classic)	rs1049663
ClinGen	rs1049663
ebi	rs1049663
HLI	rs1049663
Exac	rs1049663
Gnomad	rs1049663
Varsome	rs1049663
LitVar	rs1049663
Map	rs1049663
PheGenI	rs1049663
Biobank	rs1049663
1000 genomes	rs1049663
hgdp	rs1049663
ensembl	rs1049663
geneview	rs1049663
scholar	rs1049663
google	rs1049663
pharmgkb	rs1049663
gwascentral	rs1049663
openSNP	rs1049663
23andMe	rs1049663
SNPshot	rs1049663
SNPdbe	rs1049663
MSV3d	rs1049663
GWAS Ctlg	rs1049663

GMAF

0.02663

Max Magnitude

0

ClinVar
Risk	rs1049663(T;T)
Alt	rs1049663(T;T)
Reference	Rs1049663(G;G)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31236813C>A
CLNSRC
CLNACC