rs567032648
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs567032648(C;C) |
Make rs567032648(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 49022175 |
Gene | DALRD3, MIR191, MIR425, NDUFAF3 |
is a | snp |
is | mentioned by |
dbSNP | rs567032648 |
dbSNP (classic) | rs567032648 |
ClinGen | rs567032648 |
ebi | rs567032648 |
HLI | rs567032648 |
Exac | rs567032648 |
Gnomad | rs567032648 |
Varsome | rs567032648 |
LitVar | rs567032648 |
Map | rs567032648 |
PheGenI | rs567032648 |
Biobank | rs567032648 |
1000 genomes | rs567032648 |
hgdp | rs567032648 |
ensembl | rs567032648 |
geneview | rs567032648 |
scholar | rs567032648 |
rs567032648 | |
pharmgkb | rs567032648 |
gwascentral | rs567032648 |
openSNP | rs567032648 |
23andMe | rs567032648 |
SNPshot | rs567032648 |
SNPdbe | rs567032648 |
MSV3d | rs567032648 |
GWAS Ctlg | rs567032648 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs567032648(C;C) rs567032648(G;G) |
Alt | rs567032648(C;C) rs567032648(G;G) |
Reference | Rs567032648(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MIR425 DALRD3 NDUFAF3 MIR191 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.49059608T>G |
CLNSRC | |
CLNACC | RCV000198139.1, |