rs759151952
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs759151952(-;-) |
Make rs759151952(-;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 5987265 |
Gene | PMS2 |
is a | snp |
is | mentioned by |
dbSNP | rs759151952 |
dbSNP (classic) | rs759151952 |
ClinGen | rs759151952 |
ebi | rs759151952 |
HLI | rs759151952 |
Exac | rs759151952 |
Gnomad | rs759151952 |
Varsome | rs759151952 |
LitVar | rs759151952 |
Map | rs759151952 |
PheGenI | rs759151952 |
Biobank | rs759151952 |
1000 genomes | rs759151952 |
hgdp | rs759151952 |
ensembl | rs759151952 |
geneview | rs759151952 |
scholar | rs759151952 |
rs759151952 | |
pharmgkb | rs759151952 |
gwascentral | rs759151952 |
openSNP | rs759151952 |
23andMe | rs759151952 |
SNPshot | rs759151952 |
SNPdbe | rs759151952 |
MSV3d | rs759151952 |
GWAS Ctlg | rs759151952 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759151952(-;-) |
Alt | rs759151952(-;-) |
Reference | Rs759151952(G;G) |
Significance | Pathogenic |
Disease | Lynch syndrome |
Variation | info |
Gene | PMS2 |
CLNDBN | Lynch syndrome |
Reversed | 0 |
HGVS | NC_000007.13:g.6026896delG |
CLNSRC | |
CLNACC | RCV000210104.1, |