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rs34794906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs34794906(C;C)
Make rs34794906(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270081
GeneHLA-C
is asnp
is mentioned by
dbSNPrs34794906
ebirs34794906
HLIrs34794906
Exacrs34794906
Varsomers34794906
Maprs34794906
PheGenIrs34794906
hapmaprs34794906
1000 genomesrs34794906
hgdprs34794906
ensemblrs34794906
gopubmedrs34794906
geneviewrs34794906
scholarrs34794906
googlers34794906
pharmgkbrs34794906
gwascentralrs34794906
openSNPrs34794906
23andMers34794906
23andMe allrs34794906
SNP Nexus

SNPshotrs34794906
SNPdbers34794906
MSV3drs34794906
GWAS Ctlgrs34794906
GMAF0.3806
Max Magnitude0
ClinVar
Risk rs34794906(C;C)
Alt rs34794906(C;C)
Reference rs34794906(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237858T>C
CLNSRC
CLNACC