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rs1064796335

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position38411860
GeneOTC
is asnp
is mentioned by
dbSNPrs1064796335
dbSNP (old)rs1064796335
ClinGenrs1064796335
ebirs1064796335
HLIrs1064796335
Exacrs1064796335
Gnomadrs1064796335
Varsomers1064796335
Maprs1064796335
PheGenIrs1064796335
Biobankrs1064796335
1000 genomesrs1064796335
hgdprs1064796335
ensemblrs1064796335
gopubmedrs1064796335
geneviewrs1064796335
scholarrs1064796335
googlers1064796335
pharmgkbrs1064796335
gwascentralrs1064796335
openSNPrs1064796335
23andMers1064796335
23andMe allrs1064796335
SNPshotrs1064796335
SNPdbers1064796335
MSV3drs1064796335
GWAS Ctlgrs1064796335
Max Magnitude0
ClinVar
Risk rs1064796335(T;T)
Alt rs1064796335(T;T)
Reference Rs1064796335(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271113A>T
CLNSRC
CLNACC RCV000480612.1,