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rs72558479

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558479(A;T)
Make rs72558479(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411985
GeneOTC
is asnp
is mentioned by
dbSNPrs72558479
ebirs72558479
HLIrs72558479
Exacrs72558479
Varsomers72558479
Maprs72558479
PheGenIrs72558479
hapmaprs72558479
1000 genomesrs72558479
hgdprs72558479
ensemblrs72558479
gopubmedrs72558479
geneviewrs72558479
scholarrs72558479
googlers72558479
pharmgkbrs72558479
gwascentralrs72558479
openSNPrs72558479
23andMers72558479
23andMe allrs72558479
SNP Nexus

SNPshotrs72558479
SNPdbers72558479
MSV3drs72558479
GWAS Ctlgrs72558479
Max Magnitude0
ClinVar
Risk rs72558479(T;T)
Alt rs72558479(T;T)
Reference rs72558479(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271238A>T
CLNSRC ClinVar
CLNACC RCV000083626.1,