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rs41558713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41558713(C;T)
Make rs41558713(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270225
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41558713
ebirs41558713
HLIrs41558713
Exacrs41558713
Varsomers41558713
Maprs41558713
PheGenIrs41558713
hapmaprs41558713
1000 genomesrs41558713
hgdprs41558713
ensemblrs41558713
gopubmedrs41558713
geneviewrs41558713
scholarrs41558713
googlers41558713
pharmgkbrs41558713
gwascentralrs41558713
openSNPrs41558713
23andMers41558713
23andMe allrs41558713
SNP Nexus

SNPshotrs41558713
SNPdbers41558713
MSV3drs41558713
GWAS Ctlgrs41558713
Max Magnitude0
ClinVar
Risk rs41558713(T;T)
Alt rs41558713(T;T)
Reference rs41558713(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238002G>A
CLNSRC
CLNACC