rs374239531
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs374239531(C;G) |
Make rs374239531(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 150133957 |
Gene | PDGFRB |
is a | snp |
is | mentioned by |
dbSNP | rs374239531 |
dbSNP (classic) | rs374239531 |
ClinGen | rs374239531 |
ebi | rs374239531 |
HLI | rs374239531 |
Exac | rs374239531 |
Gnomad | rs374239531 |
Varsome | rs374239531 |
LitVar | rs374239531 |
Map | rs374239531 |
PheGenI | rs374239531 |
Biobank | rs374239531 |
1000 genomes | rs374239531 |
hgdp | rs374239531 |
ensembl | rs374239531 |
geneview | rs374239531 |
scholar | rs374239531 |
rs374239531 | |
pharmgkb | rs374239531 |
gwascentral | rs374239531 |
openSNP | rs374239531 |
23andMe | rs374239531 |
SNPshot | rs374239531 |
SNPdbe | rs374239531 |
MSV3d | rs374239531 |
GWAS Ctlg | rs374239531 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs374239531(G;G) rs374239531(T;T) |
Alt | rs374239531(G;G) rs374239531(T;T) |
Reference | Rs374239531(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | PDGFRB |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000005.9:g.149513520C>T |
CLNSRC | |
CLNACC | RCV000171387.2, |