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rs41543713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41543713(C;C)
Make rs41543713(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270629
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41543713
ebirs41543713
HLIrs41543713
Exacrs41543713
Varsomers41543713
Maprs41543713
PheGenIrs41543713
hapmaprs41543713
1000 genomesrs41543713
hgdprs41543713
ensemblrs41543713
gopubmedrs41543713
geneviewrs41543713
scholarrs41543713
googlers41543713
pharmgkbrs41543713
gwascentralrs41543713
openSNPrs41543713
23andMers41543713
23andMe allrs41543713
SNP Nexus

SNPshotrs41543713
SNPdbers41543713
MSV3drs41543713
GWAS Ctlgrs41543713
GMAF0.02709
Max Magnitude0
ClinVar
Risk rs41543713(C;C)
Alt rs41543713(C;C)
Reference rs41543713(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238406C>G
CLNSRC
CLNACC