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rs72552300

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72552300(C;T)
Make rs72552300(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38352763
GeneOTC
is asnp
is mentioned by
dbSNPrs72552300
ebirs72552300
HLIrs72552300
Exacrs72552300
Varsomers72552300
Maprs72552300
PheGenIrs72552300
hapmaprs72552300
1000 genomesrs72552300
hgdprs72552300
ensemblrs72552300
gopubmedrs72552300
geneviewrs72552300
scholarrs72552300
googlers72552300
pharmgkbrs72552300
gwascentralrs72552300
openSNPrs72552300
23andMers72552300
23andMe allrs72552300
SNP Nexus

SNPshotrs72552300
SNPdbers72552300
MSV3drs72552300
GWAS Ctlgrs72552300
Max Magnitude0
ClinVar
Risk rs72552300(T;T)
Alt rs72552300(T;T)
Reference rs72552300(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38212016C>T
CLNSRC ClinVar
CLNACC RCV000083537.1,