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rs72554315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554315(C;C)
Make rs72554315(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367356
GeneOTC
is asnp
is mentioned by
dbSNPrs72554315
ebirs72554315
HLIrs72554315
Exacrs72554315
Varsomers72554315
Maprs72554315
PheGenIrs72554315
hapmaprs72554315
1000 genomesrs72554315
hgdprs72554315
ensemblrs72554315
gopubmedrs72554315
geneviewrs72554315
scholarrs72554315
googlers72554315
pharmgkbrs72554315
gwascentralrs72554315
openSNPrs72554315
23andMers72554315
23andMe allrs72554315
SNP Nexus

SNPshotrs72554315
SNPdbers72554315
MSV3drs72554315
GWAS Ctlgrs72554315
Max Magnitude0
ClinVar
Risk rs72554315(C;C)
Alt rs72554315(C;C)
Reference rs72554315(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226609T>C
CLNSRC ClinVar
CLNACC RCV000083343.1,