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rs72558459

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTGA;CTGA) 0 common in clinvar
(GACT;GACT) 0 common in clinvar
(I;I) 0
Make rs72558459(-;-)
Make rs72558459(-;GACT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411883
GeneOTC
is asnp
is mentioned by
dbSNPrs72558459
ebirs72558459
HLIrs72558459
Exacrs72558459
Varsomers72558459
Maprs72558459
PheGenIrs72558459
hapmaprs72558459
1000 genomesrs72558459
hgdprs72558459
ensemblrs72558459
gopubmedrs72558459
geneviewrs72558459
scholarrs72558459
googlers72558459
pharmgkbrs72558459
gwascentralrs72558459
openSNPrs72558459
23andMers72558459
23andMe allrs72558459
SNP Nexus

SNPshotrs72558459
SNPdbers72558459
MSV3drs72558459
GWAS Ctlgrs72558459
Max Magnitude0
ClinVar
Risk rs72558459(;)
Alt rs72558459(;)
Reference rs72558459(CTGA;CTGA)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271136_38271139delGACT
CLNSRC ClinVar
CLNACC RCV000083595.1,