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rs11547350

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11547350(C;T)
Make rs11547350(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271191
GeneHLA-C
is asnp
is mentioned by
dbSNPrs11547350
ebirs11547350
HLIrs11547350
Exacrs11547350
Varsomers11547350
Maprs11547350
PheGenIrs11547350
hapmaprs11547350
1000 genomesrs11547350
hgdprs11547350
ensemblrs11547350
gopubmedrs11547350
geneviewrs11547350
scholarrs11547350
googlers11547350
pharmgkbrs11547350
gwascentralrs11547350
openSNPrs11547350
23andMers11547350
23andMe allrs11547350
SNP Nexus

SNPshotrs11547350
SNPdbers11547350
MSV3drs11547350
GWAS Ctlgrs11547350
Max Magnitude0
ClinVar
Risk rs11547350(G,T;G,T)
Alt rs11547350(G,T;G,T)
Reference rs11547350(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238968G>A; NC_000006.11:g.31238968G>C
CLNSRC
CLNACC