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rs72556252

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556252(C;C)
Make rs72556252(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401280
GeneOTC
is asnp
is mentioned by
dbSNPrs72556252
ebirs72556252
HLIrs72556252
Exacrs72556252
Varsomers72556252
Maprs72556252
PheGenIrs72556252
hapmaprs72556252
1000 genomesrs72556252
hgdprs72556252
ensemblrs72556252
gopubmedrs72556252
geneviewrs72556252
scholarrs72556252
googlers72556252
pharmgkbrs72556252
gwascentralrs72556252
openSNPrs72556252
23andMers72556252
23andMe allrs72556252
SNP Nexus

SNPshotrs72556252
SNPdbers72556252
MSV3drs72556252
GWAS Ctlgrs72556252
Max Magnitude0
ClinVar
Risk rs72556252(C;C)
Alt rs72556252(C;C)
Reference rs72556252(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260533T>C
CLNSRC ClinVar
CLNACC RCV000083421.1,