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rs72558458

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs72558458(-;-)
Make rs72558458(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411876
GeneOTC
is asnp
is mentioned by
dbSNPrs72558458
ebirs72558458
HLIrs72558458
Exacrs72558458
Varsomers72558458
Maprs72558458
PheGenIrs72558458
hapmaprs72558458
1000 genomesrs72558458
hgdprs72558458
ensemblrs72558458
gopubmedrs72558458
geneviewrs72558458
scholarrs72558458
googlers72558458
pharmgkbrs72558458
gwascentralrs72558458
openSNPrs72558458
23andMers72558458
23andMe allrs72558458
SNP Nexus

SNPshotrs72558458
SNPdbers72558458
MSV3drs72558458
GWAS Ctlgrs72558458
Max Magnitude0
ClinVar
Risk rs72558458(;)
Alt rs72558458(;)
Reference rs72558458(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271129delT
CLNSRC ClinVar
CLNACC RCV000083594.1,