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rs1049724

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1049724(A;A)
Make rs1049724(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269085
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1049724
ebirs1049724
HLIrs1049724
Exacrs1049724
Varsomers1049724
Maprs1049724
PheGenIrs1049724
hapmaprs1049724
1000 genomesrs1049724
hgdprs1049724
ensemblrs1049724
gopubmedrs1049724
geneviewrs1049724
scholarrs1049724
googlers1049724
pharmgkbrs1049724
gwascentralrs1049724
openSNPrs1049724
23andMers1049724
23andMe allrs1049724
SNP Nexus

SNPshotrs1049724
SNPdbers1049724
MSV3drs1049724
GWAS Ctlgrs1049724
GMAF0.03444
Max Magnitude0
ClinVar
Risk rs1049724(A;A)
Alt rs1049724(A;A)
Reference Rs1049724(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31236862C>T
CLNSRC
CLNACC