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rs72558439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs72558439(-;-)
Make rs72558439(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408917
GeneOTC
is asnp
is mentioned by
dbSNPrs72558439
ebirs72558439
HLIrs72558439
Exacrs72558439
Varsomers72558439
Maprs72558439
PheGenIrs72558439
hapmaprs72558439
1000 genomesrs72558439
hgdprs72558439
ensemblrs72558439
gopubmedrs72558439
geneviewrs72558439
scholarrs72558439
googlers72558439
pharmgkbrs72558439
gwascentralrs72558439
openSNPrs72558439
23andMers72558439
23andMe allrs72558439
SNP Nexus

SNPshotrs72558439
SNPdbers72558439
MSV3drs72558439
GWAS Ctlgrs72558439
Max Magnitude0
ClinVar
Risk rs72558439(;)
Alt rs72558439(;)
Reference rs72558439(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268170delA
CLNSRC ClinVar
CLNACC RCV000083557.1,