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rs41562921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562921(A;A)
Make rs41562921(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269477
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41562921
ebirs41562921
HLIrs41562921
Exacrs41562921
Varsomers41562921
Maprs41562921
PheGenIrs41562921
hapmaprs41562921
1000 genomesrs41562921
hgdprs41562921
ensemblrs41562921
gopubmedrs41562921
geneviewrs41562921
scholarrs41562921
googlers41562921
pharmgkbrs41562921
gwascentralrs41562921
openSNPrs41562921
23andMers41562921
23andMe allrs41562921
SNP Nexus

SNPshotrs41562921
SNPdbers41562921
MSV3drs41562921
GWAS Ctlgrs41562921
GMAF0.03444
Max Magnitude0
ClinVar
Risk rs41562921(A;A)
Alt rs41562921(A;A)
Reference rs41562921(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237254C>T
CLNSRC
CLNACC