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rs116744327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs116744327(A;A)
Make rs116744327(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270141
GeneHLA-C
is asnp
is mentioned by
dbSNPrs116744327
ebirs116744327
HLIrs116744327
Exacrs116744327
Varsomers116744327
Maprs116744327
PheGenIrs116744327
hapmaprs116744327
1000 genomesrs116744327
hgdprs116744327
ensemblrs116744327
gopubmedrs116744327
geneviewrs116744327
scholarrs116744327
googlers116744327
pharmgkbrs116744327
gwascentralrs116744327
openSNPrs116744327
23andMers116744327
23andMe allrs116744327
SNP Nexus

SNPshotrs116744327
SNPdbers116744327
MSV3drs116744327
GWAS Ctlgrs116744327
GMAF0.05693
Max Magnitude0
ClinVar
Risk rs116744327(A;A)
Alt rs116744327(A;A)
Reference rs116744327(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237918G>A
CLNSRC
CLNACC