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rs72554355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs72554355(-;-)
Make rs72554355(-;TT)
Make rs72554355(TT;TT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381407
GeneOTC
is asnp
is mentioned by
dbSNPrs72554355
ebirs72554355
HLIrs72554355
Exacrs72554355
Varsomers72554355
Maprs72554355
PheGenIrs72554355
hapmaprs72554355
1000 genomesrs72554355
hgdprs72554355
ensemblrs72554355
gopubmedrs72554355
geneviewrs72554355
scholarrs72554355
googlers72554355
pharmgkbrs72554355
gwascentralrs72554355
openSNPrs72554355
23andMers72554355
23andMe allrs72554355
SNP Nexus

SNPshotrs72554355
SNPdbers72554355
MSV3drs72554355
GWAS Ctlgrs72554355
Max Magnitude0
ClinVar
Risk rs72554355(TT;TT)
Alt rs72554355(TT;TT)
Reference rs72554355(;)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240660_38240661insTT
CLNSRC ClinVar
CLNACC RCV000083407.1,