rs780787386
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs780787386(C;G) |
Make rs780787386(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 7695497 |
Gene | GDF3 |
is a | snp |
is | mentioned by |
dbSNP | rs780787386 |
dbSNP (classic) | rs780787386 |
ClinGen | rs780787386 |
ebi | rs780787386 |
HLI | rs780787386 |
Exac | rs780787386 |
Gnomad | rs780787386 |
Varsome | rs780787386 |
LitVar | rs780787386 |
Map | rs780787386 |
PheGenI | rs780787386 |
Biobank | rs780787386 |
1000 genomes | rs780787386 |
hgdp | rs780787386 |
ensembl | rs780787386 |
geneview | rs780787386 |
scholar | rs780787386 |
rs780787386 | |
pharmgkb | rs780787386 |
gwascentral | rs780787386 |
openSNP | rs780787386 |
23andMe | rs780787386 |
SNPshot | rs780787386 |
SNPdbe | rs780787386 |
MSV3d | rs780787386 |
GWAS Ctlg | rs780787386 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs780787386(G;G) rs780787386(T;T) |
Alt | rs780787386(G;G) rs780787386(T;T) |
Reference | Rs780787386(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GDF3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.7848093C>G |
CLNSRC | |
CLNACC | RCV000171205.1, |