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rs72556278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556278(C;T)
Make rs72556278(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401394
GeneOTC
is asnp
is mentioned by
dbSNPrs72556278
ebirs72556278
HLIrs72556278
Exacrs72556278
Varsomers72556278
Maprs72556278
PheGenIrs72556278
hapmaprs72556278
1000 genomesrs72556278
hgdprs72556278
ensemblrs72556278
gopubmedrs72556278
geneviewrs72556278
scholarrs72556278
googlers72556278
pharmgkbrs72556278
gwascentralrs72556278
openSNPrs72556278
23andMers72556278
23andMe allrs72556278
SNP Nexus

SNPshotrs72556278
SNPdbers72556278
MSV3drs72556278
GWAS Ctlgrs72556278
Max Magnitude0
ClinVar
Risk rs72556278(T;T)
Alt rs72556278(T;T)
Reference rs72556278(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260647C>T
CLNSRC ClinVar
CLNACC RCV000083468.1,