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rs148650077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs148650077(C;C)
Make rs148650077(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270476
GeneHLA-C
is asnp
is mentioned by
dbSNPrs148650077
ebirs148650077
HLIrs148650077
Exacrs148650077
Varsomers148650077
Maprs148650077
PheGenIrs148650077
hapmaprs148650077
1000 genomesrs148650077
hgdprs148650077
ensemblrs148650077
gopubmedrs148650077
geneviewrs148650077
scholarrs148650077
googlers148650077
pharmgkbrs148650077
gwascentralrs148650077
openSNPrs148650077
23andMers148650077
23andMe allrs148650077
SNP Nexus

SNPshotrs148650077
SNPdbers148650077
MSV3drs148650077
GWAS Ctlgrs148650077
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs148650077(C;C)
Alt rs148650077(C;C)
Reference rs148650077(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238253T>C
CLNSRC
CLNACC