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rs74972087

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74972087(A;A)
Make rs74972087(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271665
GeneHLA-C
is asnp
is mentioned by
dbSNPrs74972087
ebirs74972087
HLIrs74972087
Exacrs74972087
Varsomers74972087
Maprs74972087
PheGenIrs74972087
hapmaprs74972087
1000 genomesrs74972087
hgdprs74972087
ensemblrs74972087
gopubmedrs74972087
geneviewrs74972087
scholarrs74972087
googlers74972087
pharmgkbrs74972087
gwascentralrs74972087
openSNPrs74972087
23andMers74972087
23andMe allrs74972087
SNP Nexus

SNPshotrs74972087
SNPdbers74972087
MSV3drs74972087
GWAS Ctlgrs74972087
Max Magnitude0
ClinVar
Risk rs74972087(A,T;A,T)
Alt rs74972087(A,T;A,T)
Reference rs74972087(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239442G>A; NC_000006.11:g.31239442G>T
CLNSRC
CLNACC