rs780724594
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs780724594(C;C) |
Make rs780724594(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 68294680 |
Gene | PIK3R1 |
is a | snp |
is | mentioned by |
dbSNP | rs780724594 |
dbSNP (classic) | rs780724594 |
ClinGen | rs780724594 |
ebi | rs780724594 |
HLI | rs780724594 |
Exac | rs780724594 |
Gnomad | rs780724594 |
Varsome | rs780724594 |
LitVar | rs780724594 |
Map | rs780724594 |
PheGenI | rs780724594 |
Biobank | rs780724594 |
1000 genomes | rs780724594 |
hgdp | rs780724594 |
ensembl | rs780724594 |
geneview | rs780724594 |
scholar | rs780724594 |
rs780724594 | |
pharmgkb | rs780724594 |
gwascentral | rs780724594 |
openSNP | rs780724594 |
23andMe | rs780724594 |
SNPshot | rs780724594 |
SNPdbe | rs780724594 |
MSV3d | rs780724594 |
GWAS Ctlg | rs780724594 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs780724594(C;C) |
Alt | rs780724594(C;C) |
Reference | Rs780724594(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PIK3R1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.67590508T>C |
CLNSRC | |
CLNACC | RCV000443391.1, |