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rs72554314

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
Make rs72554314(-;G)
Make rs72554314(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367353
GeneOTC
is asnp
is mentioned by
dbSNPrs72554314
ebirs72554314
HLIrs72554314
Exacrs72554314
Varsomers72554314
Maprs72554314
PheGenIrs72554314
hapmaprs72554314
1000 genomesrs72554314
hgdprs72554314
ensemblrs72554314
gopubmedrs72554314
geneviewrs72554314
scholarrs72554314
googlers72554314
pharmgkbrs72554314
gwascentralrs72554314
openSNPrs72554314
23andMers72554314
23andMe allrs72554314
SNP Nexus

SNPshotrs72554314
SNPdbers72554314
MSV3drs72554314
GWAS Ctlgrs72554314
Max Magnitude0
ClinVar
Risk rs72554314(G;G)
Alt rs72554314(G;G)
Reference rs72554314(;)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226606_38226607insG
CLNSRC ClinVar
CLNACC RCV000083342.1,