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rs72554357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs72554357(-;-)
Make rs72554357(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381418
GeneOTC
is asnp
is mentioned by
dbSNPrs72554357
ebirs72554357
HLIrs72554357
Exacrs72554357
Varsomers72554357
Maprs72554357
PheGenIrs72554357
hapmaprs72554357
1000 genomesrs72554357
hgdprs72554357
ensemblrs72554357
gopubmedrs72554357
geneviewrs72554357
scholarrs72554357
googlers72554357
pharmgkbrs72554357
gwascentralrs72554357
openSNPrs72554357
23andMers72554357
23andMe allrs72554357
SNP Nexus

SNPshotrs72554357
SNPdbers72554357
MSV3drs72554357
GWAS Ctlgrs72554357
Max Magnitude0
ClinVar
Risk rs72554357(;)
Alt rs72554357(;)
Reference rs72554357(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240671delG
CLNSRC ClinVar
CLNACC RCV000083409.1,