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rs41540812

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41540812(A;A)
Make rs41540812(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270651
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41540812
ebirs41540812
HLIrs41540812
Exacrs41540812
Varsomers41540812
Maprs41540812
PheGenIrs41540812
hapmaprs41540812
1000 genomesrs41540812
hgdprs41540812
ensemblrs41540812
gopubmedrs41540812
geneviewrs41540812
scholarrs41540812
googlers41540812
pharmgkbrs41540812
gwascentralrs41540812
openSNPrs41540812
23andMers41540812
23andMe allrs41540812
SNP Nexus

SNPshotrs41540812
SNPdbers41540812
MSV3drs41540812
GWAS Ctlgrs41540812
GMAF0.02709
Max Magnitude0
ClinVar
Risk rs41540812(A;A)
Alt rs41540812(A;A)
Reference rs41540812(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238428A>T
CLNSRC
CLNACC