rs753424199
From SNPedia
Merged into | rs199422137 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs753424199(-;-) |
Make rs753424199(-;CT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 197143097 |
Gene | ASPM |
is a | snp |
is | mentioned by |
dbSNP | rs753424199 |
dbSNP (classic) | rs753424199 |
ClinGen | rs753424199 |
ebi | rs753424199 |
HLI | rs753424199 |
Exac | rs753424199 |
Gnomad | rs753424199 |
Varsome | rs753424199 |
LitVar | rs753424199 |
Map | rs753424199 |
PheGenI | rs753424199 |
Biobank | rs753424199 |
1000 genomes | rs753424199 |
hgdp | rs753424199 |
ensembl | rs753424199 |
geneview | rs753424199 |
scholar | rs753424199 |
rs753424199 | |
pharmgkb | rs753424199 |
gwascentral | rs753424199 |
openSNP | rs753424199 |
23andMe | rs753424199 |
SNPshot | rs753424199 |
SNPdbe | rs753424199 |
MSV3d | rs753424199 |
GWAS Ctlg | rs753424199 |
Status | Merged into rs199422137 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs753424199(CT;CT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ASPM |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.197112227_197112228delCT |
CLNSRC | |
CLNACC | RCV000219412.1, |