Have questions? Visit https://www.reddit.com/r/SNPedia

rs77085094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs77085094(A;A)
Make rs77085094(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270957
GeneHLA-C
is asnp
is mentioned by
dbSNPrs77085094
ebirs77085094
HLIrs77085094
Exacrs77085094
Varsomers77085094
Maprs77085094
PheGenIrs77085094
hapmaprs77085094
1000 genomesrs77085094
hgdprs77085094
ensemblrs77085094
gopubmedrs77085094
geneviewrs77085094
scholarrs77085094
googlers77085094
pharmgkbrs77085094
gwascentralrs77085094
openSNPrs77085094
23andMers77085094
23andMe allrs77085094
SNP Nexus

SNPshotrs77085094
SNPdbers77085094
MSV3drs77085094
GWAS Ctlgrs77085094
Max Magnitude0
ClinVar
Risk rs77085094(A;A)
Alt rs77085094(A;A)
Reference rs77085094(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238734C>T
CLNSRC
CLNACC