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rs72558472

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558472(C;T)
Make rs72558472(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411947
GeneOTC
is asnp
is mentioned by
dbSNPrs72558472
ebirs72558472
HLIrs72558472
Exacrs72558472
Varsomers72558472
Maprs72558472
PheGenIrs72558472
hapmaprs72558472
1000 genomesrs72558472
hgdprs72558472
ensemblrs72558472
gopubmedrs72558472
geneviewrs72558472
scholarrs72558472
googlers72558472
pharmgkbrs72558472
gwascentralrs72558472
openSNPrs72558472
23andMers72558472
23andMe allrs72558472
SNP Nexus

SNPshotrs72558472
SNPdbers72558472
MSV3drs72558472
GWAS Ctlgrs72558472
Max Magnitude0
ClinVar
Risk rs72558472(T;T)
Alt rs72558472(T;T)
Reference rs72558472(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271200C>T
CLNSRC ClinVar
CLNACC RCV000083619.1,