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rs72556262

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556262(A;T)
Make rs72556262(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401318
GeneOTC
is asnp
is mentioned by
dbSNPrs72556262
ebirs72556262
HLIrs72556262
Exacrs72556262
Varsomers72556262
Maprs72556262
PheGenIrs72556262
hapmaprs72556262
1000 genomesrs72556262
hgdprs72556262
ensemblrs72556262
gopubmedrs72556262
geneviewrs72556262
scholarrs72556262
googlers72556262
pharmgkbrs72556262
gwascentralrs72556262
openSNPrs72556262
23andMers72556262
23andMe allrs72556262
SNP Nexus

SNPshotrs72556262
SNPdbers72556262
MSV3drs72556262
GWAS Ctlgrs72556262
Max Magnitude0
ClinVar
Risk rs72556262(T;T)
Alt rs72556262(T;T)
Reference rs72556262(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260571A>T
CLNSRC ClinVar
CLNACC RCV000083437.1,