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

rs72558424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558424(A;A)
Make rs72558424(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403727
GeneOTC
is asnp
is mentioned by
dbSNPrs72558424
ebirs72558424
HLIrs72558424
Exacrs72558424
Varsomers72558424
Maprs72558424
PheGenIrs72558424
hapmaprs72558424
1000 genomesrs72558424
hgdprs72558424
ensemblrs72558424
gopubmedrs72558424
geneviewrs72558424
scholarrs72558424
googlers72558424
pharmgkbrs72558424
gwascentralrs72558424
openSNPrs72558424
23andMers72558424
23andMe allrs72558424
SNP Nexus

SNPshotrs72558424
SNPdbers72558424
MSV3drs72558424
GWAS Ctlgrs72558424
Max Magnitude0
ClinVar
Risk rs72558424(A;A)
Alt rs72558424(A;A)
Reference rs72558424(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262980C>A
CLNSRC ClinVar
CLNACC RCV000083524.1,