Have questions? Visit https://www.reddit.com/r/SNPedia

rs1050344

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050344(C;T)
Make rs1050344(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270457
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050344
ebirs1050344
HLIrs1050344
Exacrs1050344
Varsomers1050344
Maprs1050344
PheGenIrs1050344
hapmaprs1050344
1000 genomesrs1050344
hgdprs1050344
ensemblrs1050344
gopubmedrs1050344
geneviewrs1050344
scholarrs1050344
googlers1050344
pharmgkbrs1050344
gwascentralrs1050344
openSNPrs1050344
23andMers1050344
23andMe allrs1050344
SNP Nexus

SNPshotrs1050344
SNPdbers1050344
MSV3drs1050344
GWAS Ctlgrs1050344
GMAF0.225
Max Magnitude0
ClinVar
Risk rs1050344(T;T)
Alt rs1050344(T;T)
Reference rs1050344(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238234G>A
CLNSRC
CLNACC