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rs72552299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs72552299(-;-)
Make rs72552299(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38352749
GeneOTC
is asnp
is mentioned by
dbSNPrs72552299
ebirs72552299
HLIrs72552299
Exacrs72552299
Varsomers72552299
Maprs72552299
PheGenIrs72552299
hapmaprs72552299
1000 genomesrs72552299
hgdprs72552299
ensemblrs72552299
gopubmedrs72552299
geneviewrs72552299
scholarrs72552299
googlers72552299
pharmgkbrs72552299
gwascentralrs72552299
openSNPrs72552299
23andMers72552299
23andMe allrs72552299
SNP Nexus

SNPshotrs72552299
SNPdbers72552299
MSV3drs72552299
GWAS Ctlgrs72552299
Max Magnitude0
ClinVar
Risk rs72552299(;)
Alt rs72552299(;)
Reference rs72552299(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38212002delA
CLNSRC ClinVar
CLNACC RCV000083479.1,