rs587776800
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CA;CA) | 0 | common in clinvar |
Make rs587776800(-;-) |
Make rs587776800(-;CA) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 19978420 |
Gene | PLA2G2A |
is a | snp |
is | mentioned by |
dbSNP | rs587776800 |
dbSNP (classic) | rs587776800 |
ClinGen | rs587776800 |
ebi | rs587776800 |
HLI | rs587776800 |
Exac | rs587776800 |
Gnomad | rs587776800 |
Varsome | rs587776800 |
LitVar | rs587776800 |
Map | rs587776800 |
PheGenI | rs587776800 |
Biobank | rs587776800 |
1000 genomes | rs587776800 |
hgdp | rs587776800 |
ensembl | rs587776800 |
geneview | rs587776800 |
scholar | rs587776800 |
rs587776800 | |
pharmgkb | rs587776800 |
gwascentral | rs587776800 |
openSNP | rs587776800 |
23andMe | rs587776800 |
SNPshot | rs587776800 |
SNPdbe | rs587776800 |
MSV3d | rs587776800 |
GWAS Ctlg | rs587776800 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776800(-;-) |
Alt | rs587776800(-;-) |
Reference | Rs587776800(CA;CA) |
Significance | Pathogenic |
Disease | Familial colorectal cancer |
Variation | info |
Gene | PLA2G2A |
CLNDBN | Familial colorectal cancer |
Reversed | 0 |
HGVS | NC_000001.10:g.20304913_20304914delCA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014605.24, |