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rs72556259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556259(C;C)
Make rs72556259(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401304
GeneOTC
is asnp
is mentioned by
dbSNPrs72556259
ebirs72556259
HLIrs72556259
Exacrs72556259
Varsomers72556259
Maprs72556259
PheGenIrs72556259
hapmaprs72556259
1000 genomesrs72556259
hgdprs72556259
ensemblrs72556259
gopubmedrs72556259
geneviewrs72556259
scholarrs72556259
googlers72556259
pharmgkbrs72556259
gwascentralrs72556259
openSNPrs72556259
23andMers72556259
23andMe allrs72556259
SNP Nexus

SNPshotrs72556259
SNPdbers72556259
MSV3drs72556259
GWAS Ctlgrs72556259
Max Magnitude0
ClinVar
Risk rs72556259(C;C)
Alt rs72556259(C;C)
Reference rs72556259(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260557T>C
CLNSRC ClinVar
CLNACC RCV000083430.1,