rs1057518268
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AA;AA) | 0 | common in clinvar |
Make rs1057518268(-;-) |
Make rs1057518268(-;AA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 197142525 |
Gene | ASPM |
is a | snp |
is | mentioned by |
dbSNP | rs1057518268 |
dbSNP (classic) | rs1057518268 |
ClinGen | rs1057518268 |
ebi | rs1057518268 |
HLI | rs1057518268 |
Exac | rs1057518268 |
Gnomad | rs1057518268 |
Varsome | rs1057518268 |
LitVar | rs1057518268 |
Map | rs1057518268 |
PheGenI | rs1057518268 |
Biobank | rs1057518268 |
1000 genomes | rs1057518268 |
hgdp | rs1057518268 |
ensembl | rs1057518268 |
geneview | rs1057518268 |
scholar | rs1057518268 |
rs1057518268 | |
pharmgkb | rs1057518268 |
gwascentral | rs1057518268 |
openSNP | rs1057518268 |
23andMe | rs1057518268 |
SNPshot | rs1057518268 |
SNPdbe | rs1057518268 |
MSV3d | rs1057518268 |
GWAS Ctlg | rs1057518268 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518268(-;-) |
Alt | rs1057518268(-;-) |
Reference | Rs1057518268(AA;AA) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ASPM |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.197111655_197111656delTT |
CLNSRC | |
CLNACC | RCV000413189.1, |