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rs1050180

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1050180(A;G)
Make rs1050180(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270056
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050180
ebirs1050180
HLIrs1050180
Exacrs1050180
Varsomers1050180
Maprs1050180
PheGenIrs1050180
hapmaprs1050180
1000 genomesrs1050180
hgdprs1050180
ensemblrs1050180
gopubmedrs1050180
geneviewrs1050180
scholarrs1050180
googlers1050180
pharmgkbrs1050180
gwascentralrs1050180
openSNPrs1050180
23andMers1050180
23andMe allrs1050180
SNP Nexus

SNPshotrs1050180
SNPdbers1050180
MSV3drs1050180
GWAS Ctlgrs1050180
GMAF0.2259
Max Magnitude0
ClinVar
Risk rs1050180(G,T;G,T)
Alt rs1050180(G,T;G,T)
Reference rs1050180(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237833T>A; NC_000006.11:g.31237833T>C
CLNSRC
CLNACC