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

rs72558471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558471(C;C)
Make rs72558471(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411941
GeneOTC
is asnp
is mentioned by
dbSNPrs72558471
ebirs72558471
HLIrs72558471
Exacrs72558471
Varsomers72558471
Maprs72558471
PheGenIrs72558471
hapmaprs72558471
1000 genomesrs72558471
hgdprs72558471
ensemblrs72558471
gopubmedrs72558471
geneviewrs72558471
scholarrs72558471
googlers72558471
pharmgkbrs72558471
gwascentralrs72558471
openSNPrs72558471
23andMers72558471
23andMe allrs72558471
SNP Nexus

SNPshotrs72558471
SNPdbers72558471
MSV3drs72558471
GWAS Ctlgrs72558471
Max Magnitude0
ClinVar
Risk rs72558471(C;C)
Alt rs72558471(C;C)
Reference rs72558471(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271194T>C
CLNSRC ClinVar
CLNACC RCV000083617.1,