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rs72556260

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556260(C;C)
Make rs72556260(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401306
GeneOTC
is asnp
is mentioned by
dbSNPrs72556260
ebirs72556260
HLIrs72556260
Exacrs72556260
Varsomers72556260
Maprs72556260
PheGenIrs72556260
hapmaprs72556260
1000 genomesrs72556260
hgdprs72556260
ensemblrs72556260
gopubmedrs72556260
geneviewrs72556260
scholarrs72556260
googlers72556260
pharmgkbrs72556260
gwascentralrs72556260
openSNPrs72556260
23andMers72556260
23andMe allrs72556260
SNP Nexus

SNPshotrs72556260
SNPdbers72556260
MSV3drs72556260
GWAS Ctlgrs72556260
Max Magnitude0
ClinVar
Risk rs72556260(C;C)
Alt rs72556260(C;C)
Reference rs72556260(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260559G>C
CLNSRC ClinVar
CLNACC RCV000083431.1,