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rs72558411

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558411(A;G)
Make rs72558411(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403690
GeneOTC
is asnp
is mentioned by
dbSNPrs72558411
ebirs72558411
HLIrs72558411
Exacrs72558411
Varsomers72558411
Maprs72558411
PheGenIrs72558411
hapmaprs72558411
1000 genomesrs72558411
hgdprs72558411
ensemblrs72558411
gopubmedrs72558411
geneviewrs72558411
scholarrs72558411
googlers72558411
pharmgkbrs72558411
gwascentralrs72558411
openSNPrs72558411
23andMers72558411
23andMe allrs72558411
SNP Nexus

SNPshotrs72558411
SNPdbers72558411
MSV3drs72558411
GWAS Ctlgrs72558411
Max Magnitude0
ClinVar
Risk rs72558411(G;G)
Alt rs72558411(G;G)
Reference rs72558411(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262943A>G
CLNSRC ClinVar
CLNACC RCV000083512.1,