rs66459704

Orientation

plus

Stabilized

plus

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

Make rs66459704(C;C)

Make rs66459704(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31269660

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs66459704
dbSNP (classic)	rs66459704
ClinGen	rs66459704
ebi	rs66459704
HLI	rs66459704
Exac	rs66459704
Gnomad	rs66459704
Varsome	rs66459704
LitVar	rs66459704
Map	rs66459704
PheGenI	rs66459704
Biobank	rs66459704
1000 genomes	rs66459704
hgdp	rs66459704
ensembl	rs66459704
geneview	rs66459704
scholar	rs66459704
google	rs66459704
pharmgkb	rs66459704
gwascentral	rs66459704
openSNP	rs66459704
23andMe	rs66459704
SNPshot	rs66459704
SNPdbe	rs66459704
MSV3d	rs66459704
GWAS Ctlg	rs66459704

GMAF

0.2204

Max Magnitude

0

ClinVar
Risk	rs66459704(C;C)
Alt	rs66459704(C;C)
Reference	Rs66459704(T;T)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	0
HGVS	NC_000006.11:g.31237437T>C
CLNSRC
CLNACC