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rs72558420

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558420(C;T)
Make rs72558420(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403717
GeneOTC
is asnp
is mentioned by
dbSNPrs72558420
ebirs72558420
HLIrs72558420
Exacrs72558420
Varsomers72558420
Maprs72558420
PheGenIrs72558420
hapmaprs72558420
1000 genomesrs72558420
hgdprs72558420
ensemblrs72558420
gopubmedrs72558420
geneviewrs72558420
scholarrs72558420
googlers72558420
pharmgkbrs72558420
gwascentralrs72558420
openSNPrs72558420
23andMers72558420
23andMe allrs72558420
SNP Nexus

SNPshotrs72558420
SNPdbers72558420
MSV3drs72558420
GWAS Ctlgrs72558420
Max Magnitude0
ClinVar
Risk rs72558420(T;T)
Alt rs72558420(T;T)
Reference rs72558420(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262970C>T
CLNSRC ClinVar
CLNACC RCV000083520.1,