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rs72558478

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558478(A;G)
Make rs72558478(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411982
GeneOTC
is asnp
is mentioned by
dbSNPrs72558478
ebirs72558478
HLIrs72558478
Exacrs72558478
Varsomers72558478
Maprs72558478
PheGenIrs72558478
hapmaprs72558478
1000 genomesrs72558478
hgdprs72558478
ensemblrs72558478
gopubmedrs72558478
geneviewrs72558478
scholarrs72558478
googlers72558478
pharmgkbrs72558478
gwascentralrs72558478
openSNPrs72558478
23andMers72558478
23andMe allrs72558478
SNP Nexus

SNPshotrs72558478
SNPdbers72558478
MSV3drs72558478
GWAS Ctlgrs72558478
Max Magnitude0
ClinVar
Risk rs72558478(G;G)
Alt rs72558478(G;G)
Reference rs72558478(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271235A>G
CLNSRC ClinVar
CLNACC RCV000083625.1,