rs750831299
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs750831299(C;T) |
Make rs750831299(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 67609490 |
Gene | NDUFV1 |
is a | snp |
is | mentioned by |
dbSNP | rs750831299 |
dbSNP (classic) | rs750831299 |
ClinGen | rs750831299 |
ebi | rs750831299 |
HLI | rs750831299 |
Exac | rs750831299 |
Gnomad | rs750831299 |
Varsome | rs750831299 |
LitVar | rs750831299 |
Map | rs750831299 |
PheGenI | rs750831299 |
Biobank | rs750831299 |
1000 genomes | rs750831299 |
hgdp | rs750831299 |
ensembl | rs750831299 |
geneview | rs750831299 |
scholar | rs750831299 |
rs750831299 | |
pharmgkb | rs750831299 |
gwascentral | rs750831299 |
openSNP | rs750831299 |
23andMe | rs750831299 |
SNPshot | rs750831299 |
SNPdbe | rs750831299 |
MSV3d | rs750831299 |
GWAS Ctlg | rs750831299 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs750831299(T;T) |
Alt | rs750831299(T;T) |
Reference | Rs750831299(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NDUFV1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.67376961C>T |
CLNSRC | |
CLNACC | RCV000197256.1, |