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rs72558492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558492(A;G)
Make rs72558492(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421051
GeneOTC
is asnp
is mentioned by
dbSNPrs72558492
ebirs72558492
HLIrs72558492
Exacrs72558492
Varsomers72558492
Maprs72558492
PheGenIrs72558492
hapmaprs72558492
1000 genomesrs72558492
hgdprs72558492
ensemblrs72558492
gopubmedrs72558492
geneviewrs72558492
scholarrs72558492
googlers72558492
pharmgkbrs72558492
gwascentralrs72558492
openSNPrs72558492
23andMers72558492
23andMe allrs72558492
SNP Nexus

SNPshotrs72558492
SNPdbers72558492
MSV3drs72558492
GWAS Ctlgrs72558492
Max Magnitude0
ClinVar
Risk rs72558492(G;G)
Alt rs72558492(G;G)
Reference rs72558492(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280304A>G
CLNSRC ClinVar
CLNACC RCV000083326.1,