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rs140959406

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140959406(C;T)
Make rs140959406(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position45529415
GeneOPA3
is asnp
is mentioned by
dbSNPrs140959406
ebirs140959406
HLIrs140959406
Exacrs140959406
Varsomers140959406
Maprs140959406
PheGenIrs140959406
hapmaprs140959406
1000 genomesrs140959406
hgdprs140959406
ensemblrs140959406
gopubmedrs140959406
geneviewrs140959406
scholarrs140959406
googlers140959406
pharmgkbrs140959406
gwascentralrs140959406
openSNPrs140959406
23andMers140959406
23andMe allrs140959406
SNP Nexus

SNPshotrs140959406
SNPdbers140959406
MSV3drs140959406
GWAS Ctlgrs140959406
Max Magnitude0
ClinVar
Risk rs140959406(T;T)
Alt rs140959406(T;T)
Reference rs140959406(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene OPA3
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.46032673C>T
CLNSRC
CLNACC RCV000195491.1,