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rs1050371

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050371(C;T)
Make rs1050371(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271233
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050371
ebirs1050371
HLIrs1050371
Exacrs1050371
Varsomers1050371
Maprs1050371
PheGenIrs1050371
hapmaprs1050371
1000 genomesrs1050371
hgdprs1050371
ensemblrs1050371
gopubmedrs1050371
geneviewrs1050371
scholarrs1050371
googlers1050371
pharmgkbrs1050371
gwascentralrs1050371
openSNPrs1050371
23andMers1050371
23andMe allrs1050371
SNP Nexus

SNPshotrs1050371
SNPdbers1050371
MSV3drs1050371
GWAS Ctlgrs1050371
GMAF0.2544
Max Magnitude0
ClinVar
Risk rs1050371(T;T)
Alt rs1050371(T;T)
Reference rs1050371(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239010G>A
CLNSRC
CLNACC