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rs72558495

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558495(G;G)
Make rs72558495(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421078
GeneOTC
is asnp
is mentioned by
dbSNPrs72558495
ebirs72558495
HLIrs72558495
Exacrs72558495
Varsomers72558495
Maprs72558495
PheGenIrs72558495
hapmaprs72558495
1000 genomesrs72558495
hgdprs72558495
ensemblrs72558495
gopubmedrs72558495
geneviewrs72558495
scholarrs72558495
googlers72558495
pharmgkbrs72558495
gwascentralrs72558495
openSNPrs72558495
23andMers72558495
23andMe allrs72558495
SNP Nexus

SNPshotrs72558495
SNPdbers72558495
MSV3drs72558495
GWAS Ctlgrs72558495
Max Magnitude0
ClinVar
Risk rs72558495(G;G)
Alt rs72558495(G;G)
Reference rs72558495(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280331T>G
CLNSRC ClinVar
CLNACC RCV000083329.1,