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rs72556300

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556300(A;T)
Make rs72556300(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403664
GeneOTC
is asnp
is mentioned by
dbSNPrs72556300
ebirs72556300
HLIrs72556300
Exacrs72556300
Varsomers72556300
Maprs72556300
PheGenIrs72556300
hapmaprs72556300
1000 genomesrs72556300
hgdprs72556300
ensemblrs72556300
gopubmedrs72556300
geneviewrs72556300
scholarrs72556300
googlers72556300
pharmgkbrs72556300
gwascentralrs72556300
openSNPrs72556300
23andMers72556300
23andMe allrs72556300
SNP Nexus

SNPshotrs72556300
SNPdbers72556300
MSV3drs72556300
GWAS Ctlgrs72556300
Max Magnitude0
ClinVar
Risk rs72556300(T;T)
Alt rs72556300(T;T)
Reference rs72556300(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262917A>T
CLNSRC ClinVar
CLNACC RCV000083501.1,