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rs79636386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs79636386(A;A)
Make rs79636386(A;G)
Make rs79636386(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271153
GeneHLA-C
is asnp
is mentioned by
dbSNPrs79636386
ebirs79636386
HLIrs79636386
Exacrs79636386
Varsomers79636386
Maprs79636386
PheGenIrs79636386
hapmaprs79636386
1000 genomesrs79636386
hgdprs79636386
ensemblrs79636386
gopubmedrs79636386
geneviewrs79636386
scholarrs79636386
googlers79636386
pharmgkbrs79636386
gwascentralrs79636386
openSNPrs79636386
23andMers79636386
23andMe allrs79636386
SNP Nexus

SNPshotrs79636386
SNPdbers79636386
MSV3drs79636386
GWAS Ctlgrs79636386
GMAF0.3017
Max Magnitude0
ClinVar
Risk rs79636386(A,G;A,G)
Alt rs79636386(A,G;A,G)
Reference rs79636386(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238930A>C; NC_000006.11:g.31238930A>T
CLNSRC
CLNACC