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rs41561715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41561715(A;A)
Make rs41561715(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270490
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41561715
ebirs41561715
HLIrs41561715
Exacrs41561715
Varsomers41561715
Maprs41561715
PheGenIrs41561715
hapmaprs41561715
1000 genomesrs41561715
hgdprs41561715
ensemblrs41561715
gopubmedrs41561715
geneviewrs41561715
scholarrs41561715
googlers41561715
pharmgkbrs41561715
gwascentralrs41561715
openSNPrs41561715
23andMers41561715
23andMe allrs41561715
SNP Nexus

SNPshotrs41561715
SNPdbers41561715
MSV3drs41561715
GWAS Ctlgrs41561715
GMAF0.1474
Max Magnitude0
ClinVar
Risk rs41561715(A;A)
Alt rs41561715(A;A)
Reference rs41561715(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238267C>T
CLNSRC
CLNACC