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rs72552301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72552301(A;C)
Make rs72552301(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38352777
GeneOTC
is asnp
is mentioned by
dbSNPrs72552301
ebirs72552301
HLIrs72552301
Exacrs72552301
Varsomers72552301
Maprs72552301
PheGenIrs72552301
hapmaprs72552301
1000 genomesrs72552301
hgdprs72552301
ensemblrs72552301
gopubmedrs72552301
geneviewrs72552301
scholarrs72552301
googlers72552301
pharmgkbrs72552301
gwascentralrs72552301
openSNPrs72552301
23andMers72552301
23andMe allrs72552301
SNP Nexus

SNPshotrs72552301
SNPdbers72552301
MSV3drs72552301
GWAS Ctlgrs72552301
Max Magnitude0
ClinVar
Risk rs72552301(C;C)
Alt rs72552301(C;C)
Reference rs72552301(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38212030A>C
CLNSRC ClinVar
CLNACC RCV000083562.1,