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rs72556251

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs72556251(-;-)
Make rs72556251(-;TTA)
Make rs72556251(TTA;TTA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401278
GeneOTC
is asnp
is mentioned by
dbSNPrs72556251
ebirs72556251
HLIrs72556251
Exacrs72556251
Varsomers72556251
Maprs72556251
PheGenIrs72556251
hapmaprs72556251
1000 genomesrs72556251
hgdprs72556251
ensemblrs72556251
gopubmedrs72556251
geneviewrs72556251
scholarrs72556251
googlers72556251
pharmgkbrs72556251
gwascentralrs72556251
openSNPrs72556251
23andMers72556251
23andMe allrs72556251
SNP Nexus

SNPshotrs72556251
SNPdbers72556251
MSV3drs72556251
GWAS Ctlgrs72556251
Max Magnitude0
ClinVar
Risk rs72556251(TAT;TAT)
Alt rs72556251(TAT;TAT)
Reference rs72556251(;)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260531_38260532insTTA
CLNSRC ClinVar
CLNACC RCV000083420.1,