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rs41289069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41289069(A;G)
Make rs41289069(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269059
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41289069
ebirs41289069
HLIrs41289069
Exacrs41289069
Varsomers41289069
Maprs41289069
PheGenIrs41289069
hapmaprs41289069
1000 genomesrs41289069
hgdprs41289069
ensemblrs41289069
gopubmedrs41289069
geneviewrs41289069
scholarrs41289069
googlers41289069
pharmgkbrs41289069
gwascentralrs41289069
openSNPrs41289069
23andMers41289069
23andMe allrs41289069
SNP Nexus

SNPshotrs41289069
SNPdbers41289069
MSV3drs41289069
GWAS Ctlgrs41289069
Max Magnitude0
ClinVar
Risk rs41289069(G;G)
Alt rs41289069(G;G)
Reference rs41289069(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31236836A>G
CLNSRC
CLNACC