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rs72558415

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558415(A;A)
Make rs72558415(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403698
GeneOTC
is asnp
is mentioned by
dbSNPrs72558415
ebirs72558415
HLIrs72558415
Exacrs72558415
Varsomers72558415
Maprs72558415
PheGenIrs72558415
hapmaprs72558415
1000 genomesrs72558415
hgdprs72558415
ensemblrs72558415
gopubmedrs72558415
geneviewrs72558415
scholarrs72558415
googlers72558415
pharmgkbrs72558415
gwascentralrs72558415
openSNPrs72558415
23andMers72558415
23andMe allrs72558415
SNP Nexus

SNPshotrs72558415
SNPdbers72558415
MSV3drs72558415
GWAS Ctlgrs72558415
Max Magnitude0
ClinVar
Risk rs72558415(A,T;A,T)
Alt rs72558415(A,T;A,T)
Reference rs72558415(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262951C>A
CLNSRC ClinVar
CLNACC RCV000083516.1,