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rs41562012

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562012(A;A)
Make rs41562012(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270402
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41562012
ebirs41562012
HLIrs41562012
Exacrs41562012
Varsomers41562012
Maprs41562012
PheGenIrs41562012
hapmaprs41562012
1000 genomesrs41562012
hgdprs41562012
ensemblrs41562012
gopubmedrs41562012
geneviewrs41562012
scholarrs41562012
googlers41562012
pharmgkbrs41562012
gwascentralrs41562012
openSNPrs41562012
23andMers41562012
23andMe allrs41562012
SNP Nexus

SNPshotrs41562012
SNPdbers41562012
MSV3drs41562012
GWAS Ctlgrs41562012
GMAF0.01882
Max Magnitude0
ClinVar
Risk rs41562012(A;A)
Alt rs41562012(A;A)
Reference rs41562012(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238179C>T
CLNSRC
CLNACC