rs878853815
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs878853815(G;T) |
Make rs878853815(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 47408529 |
Gene | MSH2 |
is a | snp |
is | mentioned by |
dbSNP | rs878853815 |
dbSNP (classic) | rs878853815 |
ClinGen | rs878853815 |
ebi | rs878853815 |
HLI | rs878853815 |
Exac | rs878853815 |
Gnomad | rs878853815 |
Varsome | rs878853815 |
LitVar | rs878853815 |
Map | rs878853815 |
PheGenI | rs878853815 |
Biobank | rs878853815 |
1000 genomes | rs878853815 |
hgdp | rs878853815 |
ensembl | rs878853815 |
geneview | rs878853815 |
scholar | rs878853815 |
rs878853815 | |
pharmgkb | rs878853815 |
gwascentral | rs878853815 |
openSNP | rs878853815 |
23andMe | rs878853815 |
SNPshot | rs878853815 |
SNPdbe | rs878853815 |
MSV3d | rs878853815 |
GWAS Ctlg | rs878853815 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853815(T;T) |
Alt | rs878853815(T;T) |
Reference | Rs878853815(G;G) |
Significance | Pathogenic |
Disease | Lynch syndrome |
Variation | info |
Gene | MSH2 |
CLNDBN | Lynch syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.47635668G>T |
CLNSRC | |
CLNACC | RCV000228392.1, |