rs866771359
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;T) | 6 | Lynch syndrome |
(T;T) | 0 | common in clinvar |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 47806496 |
Gene | FBXO11, MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs866771359 |
dbSNP (classic) | rs866771359 |
ClinGen | rs866771359 |
ebi | rs866771359 |
HLI | rs866771359 |
Exac | rs866771359 |
Gnomad | rs866771359 |
Varsome | rs866771359 |
LitVar | rs866771359 |
Map | rs866771359 |
PheGenI | rs866771359 |
Biobank | rs866771359 |
1000 genomes | rs866771359 |
hgdp | rs866771359 |
ensembl | rs866771359 |
geneview | rs866771359 |
scholar | rs866771359 |
rs866771359 | |
pharmgkb | rs866771359 |
gwascentral | rs866771359 |
openSNP | rs866771359 |
23andMe | rs866771359 |
SNPshot | rs866771359 |
SNPdbe | rs866771359 |
MSV3d | rs866771359 |
GWAS Ctlg | rs866771359 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs866771359(ATTA;ATTA) Rs866771359(T;T) |
Alt | rs866771359(ATTA;ATTA) Rs866771359(T;T) |
Reference | Rs866771359(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | FBXO11 MSH6 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.48033635dupT |
CLNSRC | |
CLNACC | RCV000216834.1, |