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rs72556286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556286(C;C)
Make rs72556286(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401424
GeneOTC
is asnp
is mentioned by
dbSNPrs72556286
ebirs72556286
HLIrs72556286
Exacrs72556286
Varsomers72556286
Maprs72556286
PheGenIrs72556286
hapmaprs72556286
1000 genomesrs72556286
hgdprs72556286
ensemblrs72556286
gopubmedrs72556286
geneviewrs72556286
scholarrs72556286
googlers72556286
pharmgkbrs72556286
gwascentralrs72556286
openSNPrs72556286
23andMers72556286
23andMe allrs72556286
SNP Nexus

SNPshotrs72556286
SNPdbers72556286
MSV3drs72556286
GWAS Ctlgrs72556286
Max Magnitude0
ClinVar
Risk rs72556286(C;C)
Alt rs72556286(C;C)
Reference rs72556286(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260677T>C
CLNSRC ClinVar
CLNACC RCV000083478.1,