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rs72558408

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558408(C;T)
Make rs72558408(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403681
GeneOTC
is asnp
is mentioned by
dbSNPrs72558408
ebirs72558408
HLIrs72558408
Exacrs72558408
Varsomers72558408
Maprs72558408
PheGenIrs72558408
hapmaprs72558408
1000 genomesrs72558408
hgdprs72558408
ensemblrs72558408
gopubmedrs72558408
geneviewrs72558408
scholarrs72558408
googlers72558408
pharmgkbrs72558408
gwascentralrs72558408
openSNPrs72558408
23andMers72558408
23andMe allrs72558408
SNP Nexus

SNPshotrs72558408
SNPdbers72558408
MSV3drs72558408
GWAS Ctlgrs72558408
Max Magnitude0
ClinVar
Risk rs72558408(T;T)
Alt rs72558408(T;T)
Reference rs72558408(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262934C>T
CLNSRC ClinVar
CLNACC RCV000083509.1,