rs886041791
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Chromosome | 16 |
Position | 89284345 |
Gene | ANKRD11 |
is a | snp |
is | mentioned by |
dbSNP | rs886041791 |
dbSNP (classic) | rs886041791 |
ClinGen | rs886041791 |
ebi | rs886041791 |
HLI | rs886041791 |
Exac | rs886041791 |
Gnomad | rs886041791 |
Varsome | rs886041791 |
LitVar | rs886041791 |
Map | rs886041791 |
PheGenI | rs886041791 |
Biobank | rs886041791 |
1000 genomes | rs886041791 |
hgdp | rs886041791 |
ensembl | rs886041791 |
geneview | rs886041791 |
scholar | rs886041791 |
rs886041791 | |
pharmgkb | rs886041791 |
gwascentral | rs886041791 |
openSNP | rs886041791 |
23andMe | rs886041791 |
SNPshot | rs886041791 |
SNPdbe | rs886041791 |
MSV3d | rs886041791 |
GWAS Ctlg | rs886041791 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041791(T;T) |
Alt | rs886041791(T;T) |
Reference | Rs886041791(C;C) |
Significance | Pathogenic |
Disease | not provided KBG syndrome |
Variation | info |
Gene | ANKRD11 |
CLNDBN | not provided KBG syndrome |
Reversed | 1 |
HGVS | NC_000016.9:g.89350753G>A |
CLNSRC | |
CLNACC | RCV000389598.1, RCV000455520.1, |