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rs72558425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558425(C;G)
Make rs72558425(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403735
GeneOTC
is asnp
is mentioned by
dbSNPrs72558425
ebirs72558425
HLIrs72558425
Exacrs72558425
Varsomers72558425
Maprs72558425
PheGenIrs72558425
hapmaprs72558425
1000 genomesrs72558425
hgdprs72558425
ensemblrs72558425
gopubmedrs72558425
geneviewrs72558425
scholarrs72558425
googlers72558425
pharmgkbrs72558425
gwascentralrs72558425
openSNPrs72558425
23andMers72558425
23andMe allrs72558425
SNP Nexus

SNPshotrs72558425
SNPdbers72558425
MSV3drs72558425
GWAS Ctlgrs72558425
Max Magnitude0
ClinVar
Risk rs72558425(G;G)
Alt rs72558425(G;G)
Reference rs72558425(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262988C>G
CLNSRC ClinVar
CLNACC RCV000083525.1,