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rs72558428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558428(A;A)
Make rs72558428(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408751
GeneOTC
is asnp
is mentioned by
dbSNPrs72558428
ebirs72558428
HLIrs72558428
Exacrs72558428
Varsomers72558428
Maprs72558428
PheGenIrs72558428
hapmaprs72558428
1000 genomesrs72558428
hgdprs72558428
ensemblrs72558428
gopubmedrs72558428
geneviewrs72558428
scholarrs72558428
googlers72558428
pharmgkbrs72558428
gwascentralrs72558428
openSNPrs72558428
23andMers72558428
23andMe allrs72558428
SNP Nexus

SNPshotrs72558428
SNPdbers72558428
MSV3drs72558428
GWAS Ctlgrs72558428
Max Magnitude0
ClinVar
Risk rs72558428(A;A)
Alt rs72558428(A;A)
Reference rs72558428(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268004C>A
CLNSRC ClinVar
CLNACC RCV000083534.1,