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rs72558426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558426(C;T)
Make rs72558426(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403736
GeneOTC
is asnp
is mentioned by
dbSNPrs72558426
ebirs72558426
HLIrs72558426
Exacrs72558426
Varsomers72558426
Maprs72558426
PheGenIrs72558426
hapmaprs72558426
1000 genomesrs72558426
hgdprs72558426
ensemblrs72558426
gopubmedrs72558426
geneviewrs72558426
scholarrs72558426
googlers72558426
pharmgkbrs72558426
gwascentralrs72558426
openSNPrs72558426
23andMers72558426
23andMe allrs72558426
SNP Nexus

SNPshotrs72558426
SNPdbers72558426
MSV3drs72558426
GWAS Ctlgrs72558426
Max Magnitude0
ClinVar
Risk rs72558426(T;T)
Alt rs72558426(T;T)
Reference rs72558426(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262989C>T
CLNSRC ClinVar
CLNACC RCV000083526.1,