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rs41560915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41560915(A;G)
Make rs41560915(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270164
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41560915
ebirs41560915
HLIrs41560915
Exacrs41560915
Varsomers41560915
Maprs41560915
PheGenIrs41560915
hapmaprs41560915
1000 genomesrs41560915
hgdprs41560915
ensemblrs41560915
gopubmedrs41560915
geneviewrs41560915
scholarrs41560915
googlers41560915
pharmgkbrs41560915
gwascentralrs41560915
openSNPrs41560915
23andMers41560915
23andMe allrs41560915
SNP Nexus

SNPshotrs41560915
SNPdbers41560915
MSV3drs41560915
GWAS Ctlgrs41560915
Max Magnitude0
ClinVar
Risk rs41560915(G;G)
Alt rs41560915(G;G)
Reference rs41560915(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237941T>C
CLNSRC
CLNACC