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rs1050357

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050357(A;A)
Make rs1050357(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271103
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050357
ebirs1050357
HLIrs1050357
Exacrs1050357
Varsomers1050357
Maprs1050357
PheGenIrs1050357
hapmaprs1050357
1000 genomesrs1050357
hgdprs1050357
ensemblrs1050357
gopubmedrs1050357
geneviewrs1050357
scholarrs1050357
googlers1050357
pharmgkbrs1050357
gwascentralrs1050357
openSNPrs1050357
23andMers1050357
23andMe allrs1050357
SNP Nexus

SNPshotrs1050357
SNPdbers1050357
MSV3drs1050357
GWAS Ctlgrs1050357
GMAF0.1148
Max Magnitude0
ClinVar
Risk rs1050357(A;A)
Alt rs1050357(A;A)
Reference rs1050357(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238880C>T
CLNSRC
CLNACC