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rs41562916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41562916(G;G)
Make rs41562916(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271130
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41562916
ebirs41562916
HLIrs41562916
Exacrs41562916
Varsomers41562916
Maprs41562916
PheGenIrs41562916
hapmaprs41562916
1000 genomesrs41562916
hgdprs41562916
ensemblrs41562916
gopubmedrs41562916
geneviewrs41562916
scholarrs41562916
googlers41562916
pharmgkbrs41562916
gwascentralrs41562916
openSNPrs41562916
23andMers41562916
23andMe allrs41562916
SNP Nexus

SNPshotrs41562916
SNPdbers41562916
MSV3drs41562916
GWAS Ctlgrs41562916
Max Magnitude0
ClinVar
Risk rs41562916(G;G)
Alt rs41562916(G;G)
Reference rs41562916(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238907A>C
CLNSRC
CLNACC