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rs72558496

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGT;AAGT) 0 common in clinvar
(GTAA;GTAA) 0 common in clinvar
(I;I) 0
Make rs72558496(-;-)
Make rs72558496(-;AAGT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38352776
GeneOTC
is asnp
is mentioned by
dbSNPrs72558496
ebirs72558496
HLIrs72558496
Exacrs72558496
Varsomers72558496
Maprs72558496
PheGenIrs72558496
hapmaprs72558496
1000 genomesrs72558496
hgdprs72558496
ensemblrs72558496
gopubmedrs72558496
geneviewrs72558496
scholarrs72558496
googlers72558496
pharmgkbrs72558496
gwascentralrs72558496
openSNPrs72558496
23andMers72558496
23andMe allrs72558496
SNP Nexus

SNPshotrs72558496
SNPdbers72558496
MSV3drs72558496
GWAS Ctlgrs72558496
Max Magnitude0
ClinVar
Risk rs72558496(;)
Alt rs72558496(;)
Reference rs72558496(GTAA;GTAA)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38212029_38212032delAAGT
CLNSRC ClinVar
CLNACC RCV000083561.1,