rs397515612
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs397515612(A;A) |
Make rs397515612(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 3376 |
Gene | ND1 |
is a | snp |
is | mentioned by |
dbSNP | rs397515612 |
dbSNP (classic) | rs397515612 |
ClinGen | rs397515612 |
ebi | rs397515612 |
HLI | rs397515612 |
Exac | rs397515612 |
Gnomad | rs397515612 |
Varsome | rs397515612 |
LitVar | rs397515612 |
Map | rs397515612 |
PheGenI | rs397515612 |
Biobank | rs397515612 |
1000 genomes | rs397515612 |
hgdp | rs397515612 |
ensembl | rs397515612 |
geneview | rs397515612 |
scholar | rs397515612 |
rs397515612 | |
pharmgkb | rs397515612 |
gwascentral | rs397515612 |
openSNP | rs397515612 |
23andMe | rs397515612 |
SNPshot | rs397515612 |
SNPdbe | rs397515612 |
MSV3d | rs397515612 |
GWAS Ctlg | rs397515612 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397515612(A;A) |
Alt | rs397515612(A;A) |
Reference | Rs397515612(G;G) |
Significance | Pathogenic |
Disease | Leber's optic atrophy |
Variation | info |
Gene | ND1 |
CLNDBN | Leber's optic atrophy |
Reversed | 0 |
HGVS | NC_012920.1:m.3376G>A |
CLNSRC | ClinVar GeneReviews |
CLNACC | RCV000056167.1, |