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rs72556295

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556295(G;T)
Make rs72556295(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403640
GeneOTC
is asnp
is mentioned by
dbSNPrs72556295
ebirs72556295
HLIrs72556295
Exacrs72556295
Varsomers72556295
Maprs72556295
PheGenIrs72556295
hapmaprs72556295
1000 genomesrs72556295
hgdprs72556295
ensemblrs72556295
gopubmedrs72556295
geneviewrs72556295
scholarrs72556295
googlers72556295
pharmgkbrs72556295
gwascentralrs72556295
openSNPrs72556295
23andMers72556295
23andMe allrs72556295
SNP Nexus

SNPshotrs72556295
SNPdbers72556295
MSV3drs72556295
GWAS Ctlgrs72556295
Max Magnitude0
ClinVar
Risk rs72556295(T;T)
Alt rs72556295(T;T)
Reference rs72556295(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262893G>T
CLNSRC ClinVar
CLNACC RCV000083490.1,