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

rs1050366

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1050366(G;G)
Make rs1050366(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271180
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050366
ebirs1050366
HLIrs1050366
Exacrs1050366
Varsomers1050366
Maprs1050366
PheGenIrs1050366
hapmaprs1050366
1000 genomesrs1050366
hgdprs1050366
ensemblrs1050366
gopubmedrs1050366
geneviewrs1050366
scholarrs1050366
googlers1050366
pharmgkbrs1050366
gwascentralrs1050366
openSNPrs1050366
23andMers1050366
23andMe allrs1050366
SNP Nexus

SNPshotrs1050366
SNPdbers1050366
MSV3drs1050366
GWAS Ctlgrs1050366
GMAF0.3691
Max Magnitude0
ClinVar
Risk rs1050366(A;A) rs1050366(G;G)
Alt rs1050366(A;A) rs1050366(G;G)
Reference Rs1050366(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238957A>C; NC_000006.11:g.31238957A>T
CLNSRC
CLNACC