rs781691587
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs781691587(A;A) |
Make rs781691587(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 150558996 |
Gene | ADAMTSL4 |
is a | snp |
is | mentioned by |
dbSNP | rs781691587 |
dbSNP (classic) | rs781691587 |
ClinGen | rs781691587 |
ebi | rs781691587 |
HLI | rs781691587 |
Exac | rs781691587 |
Gnomad | rs781691587 |
Varsome | rs781691587 |
LitVar | rs781691587 |
Map | rs781691587 |
PheGenI | rs781691587 |
Biobank | rs781691587 |
1000 genomes | rs781691587 |
hgdp | rs781691587 |
ensembl | rs781691587 |
geneview | rs781691587 |
scholar | rs781691587 |
rs781691587 | |
pharmgkb | rs781691587 |
gwascentral | rs781691587 |
openSNP | rs781691587 |
23andMe | rs781691587 |
SNPshot | rs781691587 |
SNPdbe | rs781691587 |
MSV3d | rs781691587 |
GWAS Ctlg | rs781691587 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs781691587(A;A) |
Alt | rs781691587(A;A) |
Reference | Rs781691587(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADAMTSL4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.150531472G>A |
CLNSRC | |
CLNACC | RCV000444305.1, |