rs878855322
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AG;AG) | 0 | common in clinvar |
Make rs878855322(-;-) |
Make rs878855322(-;AG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 15 |
Position | 77029529 |
Gene | PSTPIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs878855322 |
dbSNP (classic) | rs878855322 |
ClinGen | rs878855322 |
ebi | rs878855322 |
HLI | rs878855322 |
Exac | rs878855322 |
Gnomad | rs878855322 |
Varsome | rs878855322 |
LitVar | rs878855322 |
Map | rs878855322 |
PheGenI | rs878855322 |
Biobank | rs878855322 |
1000 genomes | rs878855322 |
hgdp | rs878855322 |
ensembl | rs878855322 |
geneview | rs878855322 |
scholar | rs878855322 |
rs878855322 | |
pharmgkb | rs878855322 |
gwascentral | rs878855322 |
openSNP | rs878855322 |
23andMe | rs878855322 |
SNPshot | rs878855322 |
SNPdbe | rs878855322 |
MSV3d | rs878855322 |
GWAS Ctlg | rs878855322 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878855322(-;-) |
Alt | rs878855322(-;-) |
Reference | Rs878855322(AG;AG) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PSTPIP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.77321870_77321871delAG |
CLNSRC | |
CLNACC | RCV000231956.1, |