rs746405080
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs746405080(A;A) |
Make rs746405080(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 13788614 |
Gene | NDUFAF5 |
is a | snp |
is | mentioned by |
dbSNP | rs746405080 |
dbSNP (classic) | rs746405080 |
ClinGen | rs746405080 |
ebi | rs746405080 |
HLI | rs746405080 |
Exac | rs746405080 |
Gnomad | rs746405080 |
Varsome | rs746405080 |
LitVar | rs746405080 |
Map | rs746405080 |
PheGenI | rs746405080 |
Biobank | rs746405080 |
1000 genomes | rs746405080 |
hgdp | rs746405080 |
ensembl | rs746405080 |
geneview | rs746405080 |
scholar | rs746405080 |
rs746405080 | |
pharmgkb | rs746405080 |
gwascentral | rs746405080 |
openSNP | rs746405080 |
23andMe | rs746405080 |
SNPshot | rs746405080 |
SNPdbe | rs746405080 |
MSV3d | rs746405080 |
GWAS Ctlg | rs746405080 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs746405080(A;A) |
Alt | rs746405080(A;A) |
Reference | Rs746405080(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | NDUFAF5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.13769260G>A |
CLNSRC | |
CLNACC | RCV000197446.1, |