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rs72556264

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs72556264(-;-)
Make rs72556264(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401337
GeneOTC
is asnp
is mentioned by
dbSNPrs72556264
ebirs72556264
HLIrs72556264
Exacrs72556264
Varsomers72556264
Maprs72556264
PheGenIrs72556264
hapmaprs72556264
1000 genomesrs72556264
hgdprs72556264
ensemblrs72556264
gopubmedrs72556264
geneviewrs72556264
scholarrs72556264
googlers72556264
pharmgkbrs72556264
gwascentralrs72556264
openSNPrs72556264
23andMers72556264
23andMe allrs72556264
SNP Nexus

SNPshotrs72556264
SNPdbers72556264
MSV3drs72556264
GWAS Ctlgrs72556264
Max Magnitude0
ClinVar
Risk rs72556264(;)
Alt rs72556264(;)
Reference rs72556264(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260590delC
CLNSRC ClinVar
CLNACC RCV000083443.1,