rs41555616

Orientation

plus

Stabilized

plus

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

Make rs41555616(C;G)

Make rs41555616(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

31271081

is a	snp
is	mentioned by
dbSNP	rs41555616
dbSNP (classic)	rs41555616
ClinGen	rs41555616
ebi	rs41555616
HLI	rs41555616
Exac	rs41555616
Gnomad	rs41555616
Varsome	rs41555616
LitVar	rs41555616
Map	rs41555616
PheGenI	rs41555616
Biobank	rs41555616
1000 genomes	rs41555616
hgdp	rs41555616
ensembl	rs41555616
geneview	rs41555616
scholar	rs41555616
google	rs41555616
pharmgkb	rs41555616
gwascentral	rs41555616
openSNP	rs41555616
23andMe	rs41555616
SNPshot	rs41555616
SNPdbe	rs41555616
MSV3d	rs41555616
GWAS Ctlg	rs41555616

Max Magnitude

0

ClinVar
Risk	rs41555616(G;G)
Alt	rs41555616(G;G)
Reference	Rs41555616(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31238859G>C
CLNSRC
CLNACC