rs863225406
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;CT) | 6 | Lynch syndrome |
(TC;TC) | 0 | common in clinvar |
Make rs863225406(-;-) |
Make rs863225406(CT;CT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 47803485 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs863225406 |
dbSNP (classic) | rs863225406 |
ClinGen | rs863225406 |
ebi | rs863225406 |
HLI | rs863225406 |
Exac | rs863225406 |
Gnomad | rs863225406 |
Varsome | rs863225406 |
LitVar | rs863225406 |
Map | rs863225406 |
PheGenI | rs863225406 |
Biobank | rs863225406 |
1000 genomes | rs863225406 |
hgdp | rs863225406 |
ensembl | rs863225406 |
geneview | rs863225406 |
scholar | rs863225406 |
rs863225406 | |
pharmgkb | rs863225406 |
gwascentral | rs863225406 |
openSNP | rs863225406 |
23andMe | rs863225406 |
SNPshot | rs863225406 |
SNPdbe | rs863225406 |
MSV3d | rs863225406 |
GWAS Ctlg | rs863225406 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs863225406(-;-) |
Alt | rs863225406(-;-) |
Reference | Rs863225406(TC;TC) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MSH6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.48030624_48030625delCT |
CLNSRC | |
CLNACC | RCV000201961.1, |