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rs72558117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558117(A;A)
Make rs72558117(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356281
GeneHLA-B
is asnp
is mentioned by
dbSNPrs72558117
ebirs72558117
HLIrs72558117
Exacrs72558117
Varsomers72558117
Maprs72558117
PheGenIrs72558117
hapmaprs72558117
1000 genomesrs72558117
hgdprs72558117
ensemblrs72558117
gopubmedrs72558117
geneviewrs72558117
scholarrs72558117
googlers72558117
pharmgkbrs72558117
gwascentralrs72558117
openSNPrs72558117
23andMers72558117
23andMe allrs72558117
SNP Nexus

SNPshotrs72558117
SNPdbers72558117
MSV3drs72558117
GWAS Ctlgrs72558117
Max Magnitude0
ClinVar
Risk rs72558117(A,G;A,G)
Alt rs72558117(A,G;A,G)
Reference rs72558117(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324058G>C; NC_000006.11:g.31324058G>T
CLNSRC
CLNACC