rs863223321
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CA;CA) | 0 | common in clinvar |
Make rs863223321(-;-) |
Make rs863223321(-;CA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 89280588 |
Gene | ANKRD11 |
is a | snp |
is | mentioned by |
dbSNP | rs863223321 |
dbSNP (classic) | rs863223321 |
ClinGen | rs863223321 |
ebi | rs863223321 |
HLI | rs863223321 |
Exac | rs863223321 |
Gnomad | rs863223321 |
Varsome | rs863223321 |
LitVar | rs863223321 |
Map | rs863223321 |
PheGenI | rs863223321 |
Biobank | rs863223321 |
1000 genomes | rs863223321 |
hgdp | rs863223321 |
ensembl | rs863223321 |
geneview | rs863223321 |
scholar | rs863223321 |
rs863223321 | |
pharmgkb | rs863223321 |
gwascentral | rs863223321 |
openSNP | rs863223321 |
23andMe | rs863223321 |
SNPshot | rs863223321 |
SNPdbe | rs863223321 |
MSV3d | rs863223321 |
GWAS Ctlg | rs863223321 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863223321(-;-) |
Alt | rs863223321(-;-) |
Reference | Rs863223321(CA;CA) |
Significance | Pathogenic |
Disease | KBG syndrome |
Variation | info |
Gene | ANKRD11 |
CLNDBN | KBG syndrome |
Reversed | 1 |
HGVS | NC_000016.9:g.89346996_89346997delTG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023877.3, |