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rs72558429

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558429(C;T)
Make rs72558429(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408776
GeneOTC
is asnp
is mentioned by
dbSNPrs72558429
ebirs72558429
HLIrs72558429
Exacrs72558429
Varsomers72558429
Maprs72558429
PheGenIrs72558429
hapmaprs72558429
1000 genomesrs72558429
hgdprs72558429
ensemblrs72558429
gopubmedrs72558429
geneviewrs72558429
scholarrs72558429
googlers72558429
pharmgkbrs72558429
gwascentralrs72558429
openSNPrs72558429
23andMers72558429
23andMe allrs72558429
SNP Nexus

SNPshotrs72558429
SNPdbers72558429
MSV3drs72558429
GWAS Ctlgrs72558429
Max Magnitude0
ClinVar
Risk rs72558429(T;T)
Alt rs72558429(T;T)
Reference rs72558429(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268029C>T
CLNSRC ClinVar
CLNACC RCV000083538.1,