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rs72558485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558485(C;G)
Make rs72558485(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421020
GeneOTC
is asnp
is mentioned by
dbSNPrs72558485
ebirs72558485
HLIrs72558485
Exacrs72558485
Varsomers72558485
Maprs72558485
PheGenIrs72558485
hapmaprs72558485
1000 genomesrs72558485
hgdprs72558485
ensemblrs72558485
gopubmedrs72558485
geneviewrs72558485
scholarrs72558485
googlers72558485
pharmgkbrs72558485
gwascentralrs72558485
openSNPrs72558485
23andMers72558485
23andMe allrs72558485
SNP Nexus

SNPshotrs72558485
SNPdbers72558485
MSV3drs72558485
GWAS Ctlgrs72558485
Max Magnitude0
ClinVar
Risk rs72558485(G;G)
Alt rs72558485(G;G)
Reference rs72558485(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280273C>G
CLNSRC ClinVar
CLNACC RCV000083317.1,