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rs41557915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41557915(G;T)
Make rs41557915(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270119
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41557915
ebirs41557915
HLIrs41557915
Exacrs41557915
Varsomers41557915
Maprs41557915
PheGenIrs41557915
hapmaprs41557915
1000 genomesrs41557915
hgdprs41557915
ensemblrs41557915
gopubmedrs41557915
geneviewrs41557915
scholarrs41557915
googlers41557915
pharmgkbrs41557915
gwascentralrs41557915
openSNPrs41557915
23andMers41557915
23andMe allrs41557915
SNP Nexus

SNPshotrs41557915
SNPdbers41557915
MSV3drs41557915
GWAS Ctlgrs41557915
GMAF0.02571
Max Magnitude0
ClinVar
Risk rs41557915(T;T)
Alt rs41557915(T;T)
Reference rs41557915(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237896C>A
CLNSRC
CLNACC