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rs79767529

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs79767529(A;A)
Make rs79767529(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270299
GeneHLA-C
is asnp
is mentioned by
dbSNPrs79767529
ebirs79767529
HLIrs79767529
Exacrs79767529
Varsomers79767529
Maprs79767529
PheGenIrs79767529
hapmaprs79767529
1000 genomesrs79767529
hgdprs79767529
ensemblrs79767529
gopubmedrs79767529
geneviewrs79767529
scholarrs79767529
googlers79767529
pharmgkbrs79767529
gwascentralrs79767529
openSNPrs79767529
23andMers79767529
23andMe allrs79767529
SNP Nexus

SNPshotrs79767529
SNPdbers79767529
MSV3drs79767529
GWAS Ctlgrs79767529
Max Magnitude0
ClinVar
Risk rs79767529(A;A)
Alt rs79767529(A;A)
Reference rs79767529(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238076G>T
CLNSRC
CLNACC