rs886039878
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs886039878(A;A) |
Make rs886039878(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 20 |
Position | 35434018 |
Gene | GDF5 |
is a | snp |
is | mentioned by |
dbSNP | rs886039878 |
dbSNP (classic) | rs886039878 |
ClinGen | rs886039878 |
ebi | rs886039878 |
HLI | rs886039878 |
Exac | rs886039878 |
Gnomad | rs886039878 |
Varsome | rs886039878 |
LitVar | rs886039878 |
Map | rs886039878 |
PheGenI | rs886039878 |
Biobank | rs886039878 |
1000 genomes | rs886039878 |
hgdp | rs886039878 |
ensembl | rs886039878 |
geneview | rs886039878 |
scholar | rs886039878 |
rs886039878 | |
pharmgkb | rs886039878 |
gwascentral | rs886039878 |
openSNP | rs886039878 |
23andMe | rs886039878 |
SNPshot | rs886039878 |
SNPdbe | rs886039878 |
MSV3d | rs886039878 |
GWAS Ctlg | rs886039878 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886039878(A;A) |
Alt | rs886039878(A;A) |
Reference | Rs886039878(G;G) |
Significance | Probable-Pathogenic |
Disease | Brachydactyly type C |
Variation | info |
Gene | GDF5 |
CLNDBN | Brachydactyly type C |
Reversed | 1 |
HGVS | NC_000020.10:g.34021816C>T |
CLNSRC | |
CLNACC | RCV000256400.1, |