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rs41562920

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41562920(A;T)
Make rs41562920(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271507
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41562920
ebirs41562920
HLIrs41562920
Exacrs41562920
Varsomers41562920
Maprs41562920
PheGenIrs41562920
hapmaprs41562920
1000 genomesrs41562920
hgdprs41562920
ensemblrs41562920
gopubmedrs41562920
geneviewrs41562920
scholarrs41562920
googlers41562920
pharmgkbrs41562920
gwascentralrs41562920
openSNPrs41562920
23andMers41562920
23andMe allrs41562920
SNP Nexus

SNPshotrs41562920
SNPdbers41562920
MSV3drs41562920
GWAS Ctlgrs41562920
Max Magnitude0
ClinVar
Risk rs41562920(T;T)
Alt rs41562920(T;T)
Reference rs41562920(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239284T>A
CLNSRC
CLNACC