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rs1050320

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050320(A;A)
Make rs1050320(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270361
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050320
dbSNP (classic)rs1050320
ClinGenrs1050320
ebirs1050320
HLIrs1050320
Exacrs1050320
Gnomadrs1050320
Varsomers1050320
LitVarrs1050320
Maprs1050320
PheGenIrs1050320
Biobankrs1050320
1000 genomesrs1050320
hgdprs1050320
ensemblrs1050320
geneviewrs1050320
scholarrs1050320
googlers1050320
pharmgkbrs1050320
gwascentralrs1050320
openSNPrs1050320
23andMers1050320
SNPshotrs1050320
SNPdbers1050320
MSV3drs1050320
GWAS Ctlgrs1050320
Max Magnitude0
ClinVar
Risk rs1050320(A;A)
Alt rs1050320(A;A)
Reference Rs1050320(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238138C>T
CLNSRC
CLNACC