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rs72554343

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs72554343(-;-)
Make rs72554343(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369850
GeneOTC
is asnp
is mentioned by
dbSNPrs72554343
ebirs72554343
HLIrs72554343
Exacrs72554343
Varsomers72554343
Maprs72554343
PheGenIrs72554343
hapmaprs72554343
1000 genomesrs72554343
hgdprs72554343
ensemblrs72554343
gopubmedrs72554343
geneviewrs72554343
scholarrs72554343
googlers72554343
pharmgkbrs72554343
gwascentralrs72554343
openSNPrs72554343
23andMers72554343
23andMe allrs72554343
SNP Nexus

SNPshotrs72554343
SNPdbers72554343
MSV3drs72554343
GWAS Ctlgrs72554343
Max Magnitude0
ClinVar
Risk rs72554343(;)
Alt rs72554343(;)
Reference rs72554343(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229103delA
CLNSRC ClinVar
CLNACC RCV000083381.1,