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rs72558460

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(TG;TG) 0 common in clinvar
Make rs72558460(-;-)
Make rs72558460(-;TG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411886
GeneOTC
is asnp
is mentioned by
dbSNPrs72558460
ebirs72558460
HLIrs72558460
Exacrs72558460
Varsomers72558460
Maprs72558460
PheGenIrs72558460
hapmaprs72558460
1000 genomesrs72558460
hgdprs72558460
ensemblrs72558460
gopubmedrs72558460
geneviewrs72558460
scholarrs72558460
googlers72558460
pharmgkbrs72558460
gwascentralrs72558460
openSNPrs72558460
23andMers72558460
23andMe allrs72558460
SNP Nexus

SNPshotrs72558460
SNPdbers72558460
MSV3drs72558460
GWAS Ctlgrs72558460
Max Magnitude0
ClinVar
Risk rs72558460(;)
Alt rs72558460(;)
Reference rs72558460(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271139_38271140delTG
CLNSRC ClinVar
CLNACC RCV000083596.1,