Have questions? Visit https://www.reddit.com/r/SNPedia

rs72558115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558115(C;T)
Make rs72558115(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356321
GeneHLA-B
is asnp
is mentioned by
dbSNPrs72558115
ebirs72558115
HLIrs72558115
Exacrs72558115
Varsomers72558115
Maprs72558115
PheGenIrs72558115
hapmaprs72558115
1000 genomesrs72558115
hgdprs72558115
ensemblrs72558115
gopubmedrs72558115
geneviewrs72558115
scholarrs72558115
googlers72558115
pharmgkbrs72558115
gwascentralrs72558115
openSNPrs72558115
23andMers72558115
23andMe allrs72558115
SNP Nexus

SNPshotrs72558115
SNPdbers72558115
MSV3drs72558115
GWAS Ctlgrs72558115
Max Magnitude0
ClinVar
Risk rs72558115(G,T;G,T)
Alt rs72558115(G,T;G,T)
Reference rs72558115(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324098G>A; NC_000006.11:g.31324098G>C
CLNSRC
CLNACC