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rs2394960

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2394960(C;T)
Make rs2394960(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269240
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2394960
ebirs2394960
HLIrs2394960
Exacrs2394960
Varsomers2394960
Maprs2394960
PheGenIrs2394960
hapmaprs2394960
1000 genomesrs2394960
hgdprs2394960
ensemblrs2394960
gopubmedrs2394960
geneviewrs2394960
scholarrs2394960
googlers2394960
pharmgkbrs2394960
gwascentralrs2394960
openSNPrs2394960
23andMers2394960
23andMe allrs2394960
SNP Nexus

SNPshotrs2394960
SNPdbers2394960
MSV3drs2394960
GWAS Ctlgrs2394960
Max Magnitude0
ClinVar
Risk rs2394960(T;T)
Alt rs2394960(T;T)
Reference rs2394960(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237017C>T
CLNSRC
CLNACC