rs587781554
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587781554(-;A) |
Make rs587781554(A;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 37020396 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs587781554 |
dbSNP (classic) | rs587781554 |
ClinGen | rs587781554 |
ebi | rs587781554 |
HLI | rs587781554 |
Exac | rs587781554 |
Gnomad | rs587781554 |
Varsome | rs587781554 |
LitVar | rs587781554 |
Map | rs587781554 |
PheGenI | rs587781554 |
Biobank | rs587781554 |
1000 genomes | rs587781554 |
hgdp | rs587781554 |
ensembl | rs587781554 |
geneview | rs587781554 |
scholar | rs587781554 |
rs587781554 | |
pharmgkb | rs587781554 |
gwascentral | rs587781554 |
openSNP | rs587781554 |
23andMe | rs587781554 |
SNPshot | rs587781554 |
SNPdbe | rs587781554 |
MSV3d | rs587781554 |
GWAS Ctlg | rs587781554 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781554(A;A) |
Alt | rs587781554(A;A) |
Reference | Rs587781554(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Lynch syndrome |
Variation | info |
Gene | MLH1 |
CLNDBN | Hereditary cancer-predisposing syndrome Lynch syndrome |
Reversed | 0 |
HGVS | NC_000003.11:g.37061887dupA |
CLNSRC | |
CLNACC | RCV000129570.2, RCV000168452.1, |