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rs72558414

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558414(A;A)
Make rs72558414(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403697
GeneOTC
is asnp
is mentioned by
dbSNPrs72558414
ebirs72558414
HLIrs72558414
Exacrs72558414
Varsomers72558414
Maprs72558414
PheGenIrs72558414
hapmaprs72558414
1000 genomesrs72558414
hgdprs72558414
ensemblrs72558414
gopubmedrs72558414
geneviewrs72558414
scholarrs72558414
googlers72558414
pharmgkbrs72558414
gwascentralrs72558414
openSNPrs72558414
23andMers72558414
23andMe allrs72558414
SNP Nexus

SNPshotrs72558414
SNPdbers72558414
MSV3drs72558414
GWAS Ctlgrs72558414
Max Magnitude0
ClinVar
Risk rs72558414(A;A)
Alt rs72558414(A;A)
Reference rs72558414(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262950G>A
CLNSRC ClinVar
CLNACC RCV000083515.1,