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rs72556270

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556270(A;G)
Make rs72556270(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401369
GeneOTC
is asnp
is mentioned by
dbSNPrs72556270
ebirs72556270
HLIrs72556270
Exacrs72556270
Varsomers72556270
Maprs72556270
PheGenIrs72556270
hapmaprs72556270
1000 genomesrs72556270
hgdprs72556270
ensemblrs72556270
gopubmedrs72556270
geneviewrs72556270
scholarrs72556270
googlers72556270
pharmgkbrs72556270
gwascentralrs72556270
openSNPrs72556270
23andMers72556270
23andMe allrs72556270
SNP Nexus

SNPshotrs72556270
SNPdbers72556270
MSV3drs72556270
GWAS Ctlgrs72556270
Max Magnitude0
ClinVar
Risk rs72556270(G;G)
Alt rs72556270(G;G)
Reference rs72556270(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260622A>G
CLNSRC ClinVar
CLNACC RCV000083454.1,