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rs72558421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558421(C;T)
Make rs72558421(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403720
GeneOTC
is asnp
is mentioned by
dbSNPrs72558421
ebirs72558421
HLIrs72558421
Exacrs72558421
Varsomers72558421
Maprs72558421
PheGenIrs72558421
hapmaprs72558421
1000 genomesrs72558421
hgdprs72558421
ensemblrs72558421
gopubmedrs72558421
geneviewrs72558421
scholarrs72558421
googlers72558421
pharmgkbrs72558421
gwascentralrs72558421
openSNPrs72558421
23andMers72558421
23andMe allrs72558421
SNP Nexus

SNPshotrs72558421
SNPdbers72558421
MSV3drs72558421
GWAS Ctlgrs72558421
Max Magnitude0
ClinVar
Risk rs72558421(T;T)
Alt rs72558421(T;T)
Reference rs72558421(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262973C>T
CLNSRC ClinVar
CLNACC RCV000083521.1,