rs767602961
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs767602961(A;A) |
Make rs767602961(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 67609604 |
Gene | NDUFV1 |
is a | snp |
is | mentioned by |
dbSNP | rs767602961 |
dbSNP (classic) | rs767602961 |
ClinGen | rs767602961 |
ebi | rs767602961 |
HLI | rs767602961 |
Exac | rs767602961 |
Gnomad | rs767602961 |
Varsome | rs767602961 |
LitVar | rs767602961 |
Map | rs767602961 |
PheGenI | rs767602961 |
Biobank | rs767602961 |
1000 genomes | rs767602961 |
hgdp | rs767602961 |
ensembl | rs767602961 |
geneview | rs767602961 |
scholar | rs767602961 |
rs767602961 | |
pharmgkb | rs767602961 |
gwascentral | rs767602961 |
openSNP | rs767602961 |
23andMe | rs767602961 |
SNPshot | rs767602961 |
SNPdbe | rs767602961 |
MSV3d | rs767602961 |
GWAS Ctlg | rs767602961 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767602961(A;A) |
Alt | rs767602961(A;A) |
Reference | Rs767602961(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | NDUFV1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.67377075G>A |
CLNSRC | |
CLNACC | RCV000199260.2, |