rs1057519399
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1057519399(-;-) |
Make rs1057519399(-;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 89281038 |
Gene | ANKRD11 |
is a | snp |
is | mentioned by |
dbSNP | rs1057519399 |
dbSNP (classic) | rs1057519399 |
ClinGen | rs1057519399 |
ebi | rs1057519399 |
HLI | rs1057519399 |
Exac | rs1057519399 |
Gnomad | rs1057519399 |
Varsome | rs1057519399 |
LitVar | rs1057519399 |
Map | rs1057519399 |
PheGenI | rs1057519399 |
Biobank | rs1057519399 |
1000 genomes | rs1057519399 |
hgdp | rs1057519399 |
ensembl | rs1057519399 |
geneview | rs1057519399 |
scholar | rs1057519399 |
rs1057519399 | |
pharmgkb | rs1057519399 |
gwascentral | rs1057519399 |
openSNP | rs1057519399 |
23andMe | rs1057519399 |
SNPshot | rs1057519399 |
SNPdbe | rs1057519399 |
MSV3d | rs1057519399 |
GWAS Ctlg | rs1057519399 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057519399(-;-) |
Alt | rs1057519399(-;-) |
Reference | Rs1057519399(T;T) |
Significance | Pathogenic |
Disease | KBG syndrome |
Variation | info |
Gene | ANKRD11 |
CLNDBN | KBG syndrome |
Reversed | 1 |
HGVS | NC_000016.9:g.89347446delA |
CLNSRC | |
CLNACC | RCV000417088.1, |