rs140959406
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs140959406(C;T) |
Make rs140959406(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 45529415 |
Gene | OPA3 |
is a | snp |
is | mentioned by |
dbSNP | rs140959406 |
dbSNP (classic) | rs140959406 |
ClinGen | rs140959406 |
ebi | rs140959406 |
HLI | rs140959406 |
Exac | rs140959406 |
Gnomad | rs140959406 |
Varsome | rs140959406 |
LitVar | rs140959406 |
Map | rs140959406 |
PheGenI | rs140959406 |
Biobank | rs140959406 |
1000 genomes | rs140959406 |
hgdp | rs140959406 |
ensembl | rs140959406 |
geneview | rs140959406 |
scholar | rs140959406 |
rs140959406 | |
pharmgkb | rs140959406 |
gwascentral | rs140959406 |
openSNP | rs140959406 |
23andMe | rs140959406 |
SNPshot | rs140959406 |
SNPdbe | rs140959406 |
MSV3d | rs140959406 |
GWAS Ctlg | rs140959406 |
Max Magnitude | 0 |
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 | RCV000195491.2, |