rs199974018
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs199974018(C;C) |
Make rs199974018(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 12811 |
Gene | ND5 |
is a | snp |
is | mentioned by |
dbSNP | rs199974018 |
dbSNP (classic) | rs199974018 |
ClinGen | rs199974018 |
ebi | rs199974018 |
HLI | rs199974018 |
Exac | rs199974018 |
Gnomad | rs199974018 |
Varsome | rs199974018 |
LitVar | rs199974018 |
Map | rs199974018 |
PheGenI | rs199974018 |
Biobank | rs199974018 |
1000 genomes | rs199974018 |
hgdp | rs199974018 |
ensembl | rs199974018 |
geneview | rs199974018 |
scholar | rs199974018 |
rs199974018 | |
pharmgkb | rs199974018 |
gwascentral | rs199974018 |
openSNP | rs199974018 |
23andMe | rs199974018 |
SNPshot | rs199974018 |
SNPdbe | rs199974018 |
MSV3d | rs199974018 |
GWAS Ctlg | rs199974018 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199974018(C;C) |
Alt | rs199974018(C;C) |
Reference | Rs199974018(T;T) |
Significance | Pathogenic |
Disease | Leber's optic atrophy |
Variation | info |
Gene | ND5 |
CLNDBN | Leber's optic atrophy |
Reversed | 0 |
HGVS | NC_012920.1:m.12811T>C |
CLNSRC | ClinVar GeneReviews |
CLNACC | RCV000055698.1, |