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rs72554353

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs72554353(-;-)
Make rs72554353(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381370
GeneOTC
is asnp
is mentioned by
dbSNPrs72554353
ebirs72554353
HLIrs72554353
Exacrs72554353
Varsomers72554353
Maprs72554353
PheGenIrs72554353
hapmaprs72554353
1000 genomesrs72554353
hgdprs72554353
ensemblrs72554353
gopubmedrs72554353
geneviewrs72554353
scholarrs72554353
googlers72554353
pharmgkbrs72554353
gwascentralrs72554353
openSNPrs72554353
23andMers72554353
23andMe allrs72554353
SNP Nexus

SNPshotrs72554353
SNPdbers72554353
MSV3drs72554353
GWAS Ctlgrs72554353
Max Magnitude0
ClinVar
Risk rs72554353(;)
Alt rs72554353(;)
Reference rs72554353(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240623delT
CLNSRC ClinVar
CLNACC RCV000083403.1,