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rs72556257

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556257(A;T)
Make rs72556257(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401295
GeneOTC
is asnp
is mentioned by
dbSNPrs72556257
ebirs72556257
HLIrs72556257
Exacrs72556257
Varsomers72556257
Maprs72556257
PheGenIrs72556257
hapmaprs72556257
1000 genomesrs72556257
hgdprs72556257
ensemblrs72556257
gopubmedrs72556257
geneviewrs72556257
scholarrs72556257
googlers72556257
pharmgkbrs72556257
gwascentralrs72556257
openSNPrs72556257
23andMers72556257
23andMe allrs72556257
SNP Nexus

SNPshotrs72556257
SNPdbers72556257
MSV3drs72556257
GWAS Ctlgrs72556257
Max Magnitude0
ClinVar
Risk rs72556257(T;T)
Alt rs72556257(T;T)
Reference rs72556257(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260548A>T
CLNSRC ClinVar
CLNACC RCV000083427.1,