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rs72554354

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs72554354(-;-)
Make rs72554354(-;GT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381401
GeneOTC
is asnp
is mentioned by
dbSNPrs72554354
ebirs72554354
HLIrs72554354
Exacrs72554354
Varsomers72554354
Maprs72554354
PheGenIrs72554354
hapmaprs72554354
1000 genomesrs72554354
hgdprs72554354
ensemblrs72554354
gopubmedrs72554354
geneviewrs72554354
scholarrs72554354
googlers72554354
pharmgkbrs72554354
gwascentralrs72554354
openSNPrs72554354
23andMers72554354
23andMe allrs72554354
SNP Nexus

SNPshotrs72554354
SNPdbers72554354
MSV3drs72554354
GWAS Ctlgrs72554354
Max Magnitude0
ClinVar
Risk rs72554354(;)
Alt rs72554354(;)
Reference rs72554354(GT;GT)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240654_38240655delGT
CLNSRC ClinVar
CLNACC RCV000083406.1,