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rs72558457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558457(-;-)
Make rs72558457(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411869
GeneOTC
is asnp
is mentioned by
dbSNPrs72558457
ebirs72558457
HLIrs72558457
Exacrs72558457
Varsomers72558457
Maprs72558457
PheGenIrs72558457
hapmaprs72558457
1000 genomesrs72558457
hgdprs72558457
ensemblrs72558457
gopubmedrs72558457
geneviewrs72558457
scholarrs72558457
googlers72558457
pharmgkbrs72558457
gwascentralrs72558457
openSNPrs72558457
23andMers72558457
23andMe allrs72558457
SNP Nexus

SNPshotrs72558457
SNPdbers72558457
MSV3drs72558457
GWAS Ctlgrs72558457
Max Magnitude0
ClinVar
Risk rs72558457(;)
Alt rs72558457(;)
Reference rs72558457(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271122delA
CLNSRC ClinVar
CLNACC RCV000083593.1,