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rs1050685

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1050685(A;C)
Make rs1050685(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271133
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050685
ebirs1050685
HLIrs1050685
Exacrs1050685
Varsomers1050685
Maprs1050685
PheGenIrs1050685
hapmaprs1050685
1000 genomesrs1050685
hgdprs1050685
ensemblrs1050685
gopubmedrs1050685
geneviewrs1050685
scholarrs1050685
googlers1050685
pharmgkbrs1050685
gwascentralrs1050685
openSNPrs1050685
23andMers1050685
23andMe allrs1050685
SNP Nexus

SNPshotrs1050685
SNPdbers1050685
MSV3drs1050685
GWAS Ctlgrs1050685
GMAF0.2227
Max Magnitude0
ClinVar
Risk rs1050685(C,G;C,G)
Alt rs1050685(C,G;C,G)
Reference rs1050685(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238910T>C; NC_000006.11:g.31238910T>G
CLNSRC
CLNACC