rs587780683
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;T) | 6 | Lynch syndrome |
(T;T) | 0 | common in clinvar |
Make rs587780683(-;-) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 37050572 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs587780683 |
dbSNP (classic) | rs587780683 |
ClinGen | rs587780683 |
ebi | rs587780683 |
HLI | rs587780683 |
Exac | rs587780683 |
Gnomad | rs587780683 |
Varsome | rs587780683 |
LitVar | rs587780683 |
Map | rs587780683 |
PheGenI | rs587780683 |
Biobank | rs587780683 |
1000 genomes | rs587780683 |
hgdp | rs587780683 |
ensembl | rs587780683 |
geneview | rs587780683 |
scholar | rs587780683 |
rs587780683 | |
pharmgkb | rs587780683 |
gwascentral | rs587780683 |
openSNP | rs587780683 |
23andMe | rs587780683 |
SNPshot | rs587780683 |
SNPdbe | rs587780683 |
MSV3d | rs587780683 |
GWAS Ctlg | rs587780683 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs587780683(-;-) |
Alt | rs587780683(-;-) |
Reference | Rs587780683(T;T) |
Significance | Probable-Pathogenic |
Disease | Lynch syndrome |
Variation | info |
Gene | MLH1 |
CLNDBN | Lynch syndrome |
Reversed | 0 |
HGVS | NC_000003.11:g.37092063delT |
CLNSRC | |
CLNACC | RCV000122975.1, |