rs797045027
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GAAA;GAAA) | 0 | common in clinvar |
Make rs797045027(-;-) |
Make rs797045027(-;GAAA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 89284141 |
Gene | ANKRD11 |
is a | snp |
is | mentioned by |
dbSNP | rs797045027 |
dbSNP (classic) | rs797045027 |
ClinGen | rs797045027 |
ebi | rs797045027 |
HLI | rs797045027 |
Exac | rs797045027 |
Gnomad | rs797045027 |
Varsome | rs797045027 |
LitVar | rs797045027 |
Map | rs797045027 |
PheGenI | rs797045027 |
Biobank | rs797045027 |
1000 genomes | rs797045027 |
hgdp | rs797045027 |
ensembl | rs797045027 |
geneview | rs797045027 |
scholar | rs797045027 |
rs797045027 | |
pharmgkb | rs797045027 |
gwascentral | rs797045027 |
openSNP | rs797045027 |
23andMe | rs797045027 |
SNPshot | rs797045027 |
SNPdbe | rs797045027 |
MSV3d | rs797045027 |
GWAS Ctlg | rs797045027 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797045027(-;-) |
Alt | rs797045027(-;-) |
Reference | Rs797045027(GAAA;GAAA) |
Significance | Pathogenic |
Disease | KBG syndrome not provided |
Variation | info |
Gene | ANKRD11 |
CLNDBN | KBG syndrome not provided |
Reversed | 1 |
HGVS | NC_000016.9:g.89350549_89350552delTTTC |
CLNSRC | Baylor College of Medicine |
CLNACC | RCV000191060.1, RCV000255252.2, |