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rs72556297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556297(G;G)
Make rs72556297(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403649
GeneOTC
is asnp
is mentioned by
dbSNPrs72556297
ebirs72556297
HLIrs72556297
Exacrs72556297
Varsomers72556297
Maprs72556297
PheGenIrs72556297
hapmaprs72556297
1000 genomesrs72556297
hgdprs72556297
ensemblrs72556297
gopubmedrs72556297
geneviewrs72556297
scholarrs72556297
googlers72556297
pharmgkbrs72556297
gwascentralrs72556297
openSNPrs72556297
23andMers72556297
23andMe allrs72556297
SNP Nexus

SNPshotrs72556297
SNPdbers72556297
MSV3drs72556297
GWAS Ctlgrs72556297
Max Magnitude0
ClinVar
Risk rs72556297(G;G)
Alt rs72556297(G;G)
Reference rs72556297(T;T)
Significance Other
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262902T>G
CLNSRC HGMD
CLNACC RCV000079086.6,