Have questions? Visit https://www.reddit.com/r/SNPedia

rs72554340

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72554340(A;G)
Make rs72554340(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369847
GeneOTC
is asnp
is mentioned by
dbSNPrs72554340
ebirs72554340
HLIrs72554340
Exacrs72554340
Varsomers72554340
Maprs72554340
PheGenIrs72554340
hapmaprs72554340
1000 genomesrs72554340
hgdprs72554340
ensemblrs72554340
gopubmedrs72554340
geneviewrs72554340
scholarrs72554340
googlers72554340
pharmgkbrs72554340
gwascentralrs72554340
openSNPrs72554340
23andMers72554340
23andMe allrs72554340
SNP Nexus

SNPshotrs72554340
SNPdbers72554340
MSV3drs72554340
GWAS Ctlgrs72554340
Max Magnitude0
ClinVar
Risk rs72554340(G;G)
Alt rs72554340(G;G)
Reference rs72554340(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229100A>G
CLNSRC ClinVar
CLNACC RCV000083378.1,