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rs72552295

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72552295(C;C)
Make rs72552295(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38352698
GeneOTC
is asnp
is mentioned by
dbSNPrs72552295
ebirs72552295
HLIrs72552295
Exacrs72552295
Varsomers72552295
Maprs72552295
PheGenIrs72552295
hapmaprs72552295
1000 genomesrs72552295
hgdprs72552295
ensemblrs72552295
gopubmedrs72552295
geneviewrs72552295
scholarrs72552295
googlers72552295
pharmgkbrs72552295
gwascentralrs72552295
openSNPrs72552295
23andMers72552295
23andMe allrs72552295
SNP Nexus

SNPshotrs72552295
SNPdbers72552295
MSV3drs72552295
GWAS Ctlgrs72552295
Max Magnitude0
ClinVar
Risk rs72552295(C;C)
Alt rs72552295(C;C)
Reference rs72552295(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38211951T>C
CLNSRC ClinVar
CLNACC RCV000083397.1,