rs878853794
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs878853794(-;AG) |
Make rs878853794(AG;AG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 37020387 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs878853794 |
dbSNP (classic) | rs878853794 |
ClinGen | rs878853794 |
ebi | rs878853794 |
HLI | rs878853794 |
Exac | rs878853794 |
Gnomad | rs878853794 |
Varsome | rs878853794 |
LitVar | rs878853794 |
Map | rs878853794 |
PheGenI | rs878853794 |
Biobank | rs878853794 |
1000 genomes | rs878853794 |
hgdp | rs878853794 |
ensembl | rs878853794 |
geneview | rs878853794 |
scholar | rs878853794 |
rs878853794 | |
pharmgkb | rs878853794 |
gwascentral | rs878853794 |
openSNP | rs878853794 |
23andMe | rs878853794 |
SNPshot | rs878853794 |
SNPdbe | rs878853794 |
MSV3d | rs878853794 |
GWAS Ctlg | rs878853794 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853794(GA;GA) |
Alt | rs878853794(GA;GA) |
Reference | Rs878853794(-;-) |
Significance | Pathogenic |
Disease | Lynch syndrome |
Variation | info |
Gene | MLH1 |
CLNDBN | Lynch syndrome |
Reversed | 0 |
HGVS | NC_000003.11:g.37061877_37061878dupAG |
CLNSRC | |
CLNACC | RCV000228583.1, |