rs387906425
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs387906425(A;A) |
Make rs387906425(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 13730 |
Gene | ND5 |
is a | snp |
is | mentioned by |
dbSNP | rs387906425 |
dbSNP (classic) | rs387906425 |
ClinGen | rs387906425 |
ebi | rs387906425 |
HLI | rs387906425 |
Exac | rs387906425 |
Gnomad | rs387906425 |
Varsome | rs387906425 |
LitVar | rs387906425 |
Map | rs387906425 |
PheGenI | rs387906425 |
Biobank | rs387906425 |
1000 genomes | rs387906425 |
hgdp | rs387906425 |
ensembl | rs387906425 |
geneview | rs387906425 |
scholar | rs387906425 |
rs387906425 | |
pharmgkb | rs387906425 |
gwascentral | rs387906425 |
openSNP | rs387906425 |
23andMe | rs387906425 |
SNPshot | rs387906425 |
SNPdbe | rs387906425 |
MSV3d | rs387906425 |
GWAS Ctlg | rs387906425 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906425(A;A) |
Alt | rs387906425(A;A) |
Reference | Rs387906425(G;G) |
Significance | Pathogenic |
Disease | Leber's optic atrophy |
Variation | info |
Gene | ND5 |
CLNDBN | Leber's optic atrophy |
Reversed | 0 |
HGVS | NC_012920.1:m.13730G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000010337.4, |