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rs72554309

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554309(C;T)
Make rs72554309(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367340
GeneOTC
is asnp
is mentioned by
dbSNPrs72554309
ebirs72554309
HLIrs72554309
Exacrs72554309
Varsomers72554309
Maprs72554309
PheGenIrs72554309
hapmaprs72554309
1000 genomesrs72554309
hgdprs72554309
ensemblrs72554309
gopubmedrs72554309
geneviewrs72554309
scholarrs72554309
googlers72554309
pharmgkbrs72554309
gwascentralrs72554309
openSNPrs72554309
23andMers72554309
23andMe allrs72554309
SNP Nexus

SNPshotrs72554309
SNPdbers72554309
MSV3drs72554309
GWAS Ctlgrs72554309
Max Magnitude0
ClinVar
Risk rs72554309(A,T;A,T)
Alt rs72554309(A,T;A,T)
Reference rs72554309(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226593C>T
CLNSRC ClinVar
CLNACC RCV000083335.1,