rs1057520208
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6.3 | Hereditary cancer predisposing syndrome |
(G;G) | 0 | common/normal |
Make rs1057520208(A;A) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 87933012 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs1057520208 |
dbSNP (classic) | rs1057520208 |
ClinGen | rs1057520208 |
ebi | rs1057520208 |
HLI | rs1057520208 |
Exac | rs1057520208 |
Gnomad | rs1057520208 |
Varsome | rs1057520208 |
LitVar | rs1057520208 |
Map | rs1057520208 |
PheGenI | rs1057520208 |
Biobank | rs1057520208 |
1000 genomes | rs1057520208 |
hgdp | rs1057520208 |
ensembl | rs1057520208 |
geneview | rs1057520208 |
scholar | rs1057520208 |
rs1057520208 | |
pharmgkb | rs1057520208 |
gwascentral | rs1057520208 |
openSNP | rs1057520208 |
23andMe | rs1057520208 |
SNPshot | rs1057520208 |
SNPdbe | rs1057520208 |
MSV3d | rs1057520208 |
GWAS Ctlg | rs1057520208 |
Max Magnitude | 6.3 |
ClinVar | |
---|---|
Risk | rs1057520208(A;A) |
Alt | rs1057520208(A;A) |
Reference | Rs1057520208(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PTEN |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.89692769G>A |
CLNSRC | |
CLNACC | RCV000434799.1, |