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rs72554313

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs72554313(-;-)
Make rs72554313(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367348
GeneOTC
is asnp
is mentioned by
dbSNPrs72554313
ebirs72554313
HLIrs72554313
Exacrs72554313
Varsomers72554313
Maprs72554313
PheGenIrs72554313
hapmaprs72554313
1000 genomesrs72554313
hgdprs72554313
ensemblrs72554313
gopubmedrs72554313
geneviewrs72554313
scholarrs72554313
googlers72554313
pharmgkbrs72554313
gwascentralrs72554313
openSNPrs72554313
23andMers72554313
23andMe allrs72554313
SNP Nexus

SNPshotrs72554313
SNPdbers72554313
MSV3drs72554313
GWAS Ctlgrs72554313
Max Magnitude0
ClinVar
Risk rs72554313(;)
Alt rs72554313(;)
Reference rs72554313(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226601delA
CLNSRC ClinVar
CLNACC RCV000083339.1,