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rs72558456

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558456(G;T)
Make rs72558456(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38409025
GeneOTC
is asnp
is mentioned by
dbSNPrs72558456
ebirs72558456
HLIrs72558456
Exacrs72558456
Varsomers72558456
Maprs72558456
PheGenIrs72558456
hapmaprs72558456
1000 genomesrs72558456
hgdprs72558456
ensemblrs72558456
gopubmedrs72558456
geneviewrs72558456
scholarrs72558456
googlers72558456
pharmgkbrs72558456
gwascentralrs72558456
openSNPrs72558456
23andMers72558456
23andMe allrs72558456
SNP Nexus

SNPshotrs72558456
SNPdbers72558456
MSV3drs72558456
GWAS Ctlgrs72558456
Max Magnitude0
ClinVar
Risk rs72558456(T;T)
Alt rs72558456(T;T)
Reference rs72558456(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268278G>T
CLNSRC ClinVar
CLNACC RCV000083592.1,