rs587782275
From SNPedia
Merged into | rs267608058 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CAGT;CAGT) | 0 | common in clinvar |
Make rs587782275(-;-) |
Make rs587782275(-;CAGT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 47800130 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs587782275 |
dbSNP (classic) | rs587782275 |
ClinGen | rs587782275 |
ebi | rs587782275 |
HLI | rs587782275 |
Exac | rs587782275 |
Gnomad | rs587782275 |
Varsome | rs587782275 |
LitVar | rs587782275 |
Map | rs587782275 |
PheGenI | rs587782275 |
Biobank | rs587782275 |
1000 genomes | rs587782275 |
hgdp | rs587782275 |
ensembl | rs587782275 |
geneview | rs587782275 |
scholar | rs587782275 |
rs587782275 | |
pharmgkb | rs587782275 |
gwascentral | rs587782275 |
openSNP | rs587782275 |
23andMe | rs587782275 |
SNPshot | rs587782275 |
SNPdbe | rs587782275 |
MSV3d | rs587782275 |
GWAS Ctlg | rs587782275 |
Status | Merged into rs267608058 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs587782275(CAGT;CAGT) |
Significance | Pathogenic |
Disease | Lynch syndrome Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | MSH6 |
CLNDBN | Lynch syndrome Hereditary cancer-predisposing syndrome not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.48027272_48027275delTCAG |
CLNSRC | International Society for Gastrointestinal Hereditary Tumours |
CLNACC | RCV000074720.2, RCV000162408.2, RCV000202111.2, |