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rs72558422

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs72558422(-;-)
Make rs72558422(-;T)
Make rs72558422(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403722
GeneOTC
is asnp
is mentioned by
dbSNPrs72558422
ClinGenrs72558422
ebirs72558422
HLIrs72558422
Exacrs72558422
Varsomers72558422
Maprs72558422
PheGenIrs72558422
hapmaprs72558422
1000 genomesrs72558422
hgdprs72558422
ensemblrs72558422
gopubmedrs72558422
geneviewrs72558422
scholarrs72558422
googlers72558422
pharmgkbrs72558422
gwascentralrs72558422
openSNPrs72558422
23andMers72558422
23andMe allrs72558422
SNP Nexus

SNPshotrs72558422
SNPdbers72558422
MSV3drs72558422
GWAS Ctlgrs72558422
Max Magnitude0
ClinVar
Risk rs72558422(T;T)
Alt rs72558422(T;T)
Reference Rs72558422(;)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262975dupT
CLNSRC ClinVar
CLNACC RCV000083522.1,