rs863224141
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CTT;CTT) | 0 | common in clinvar |
Make rs863224141(ATA;ATA) |
Make rs863224141(ATA;CTT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 193617260 |
Gene | OPA1 |
is a | snp |
is | mentioned by |
dbSNP | rs863224141 |
dbSNP (classic) | rs863224141 |
ClinGen | rs863224141 |
ebi | rs863224141 |
HLI | rs863224141 |
Exac | rs863224141 |
Gnomad | rs863224141 |
Varsome | rs863224141 |
LitVar | rs863224141 |
Map | rs863224141 |
PheGenI | rs863224141 |
Biobank | rs863224141 |
1000 genomes | rs863224141 |
hgdp | rs863224141 |
ensembl | rs863224141 |
geneview | rs863224141 |
scholar | rs863224141 |
rs863224141 | |
pharmgkb | rs863224141 |
gwascentral | rs863224141 |
openSNP | rs863224141 |
23andMe | rs863224141 |
SNPshot | rs863224141 |
SNPdbe | rs863224141 |
MSV3d | rs863224141 |
GWAS Ctlg | rs863224141 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224141(ATA;ATA) |
Alt | rs863224141(ATA;ATA) |
Reference | Rs863224141(CTT;CTT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | OPA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.193335049_193335051delCTTinsATA |
CLNSRC | |
CLNACC | RCV000199579.1, |