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rs41540712

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41540712(A;A)
Make rs41540712(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271308
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41540712
ebirs41540712
HLIrs41540712
Exacrs41540712
Varsomers41540712
Maprs41540712
PheGenIrs41540712
hapmaprs41540712
1000 genomesrs41540712
hgdprs41540712
ensemblrs41540712
gopubmedrs41540712
geneviewrs41540712
scholarrs41540712
googlers41540712
pharmgkbrs41540712
gwascentralrs41540712
openSNPrs41540712
23andMers41540712
23andMe allrs41540712
SNP Nexus

SNPshotrs41540712
SNPdbers41540712
MSV3drs41540712
GWAS Ctlgrs41540712
Max Magnitude0
ClinVar
Risk rs41540712(A,T;A,T)
Alt rs41540712(A,T;A,T)
Reference rs41540712(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239085C>A; NC_000006.11:g.31239085C>T
CLNSRC
CLNACC