rs786203924
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TA;TA) | 0 | common in clinvar |
Make rs786203924(-;-) |
Make rs786203924(-;AT) |
Make rs786203924(AT;AT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 47800889 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs786203924 |
dbSNP (classic) | rs786203924 |
ClinGen | rs786203924 |
ebi | rs786203924 |
HLI | rs786203924 |
Exac | rs786203924 |
Gnomad | rs786203924 |
Varsome | rs786203924 |
LitVar | rs786203924 |
Map | rs786203924 |
PheGenI | rs786203924 |
Biobank | rs786203924 |
1000 genomes | rs786203924 |
hgdp | rs786203924 |
ensembl | rs786203924 |
geneview | rs786203924 |
scholar | rs786203924 |
rs786203924 | |
pharmgkb | rs786203924 |
gwascentral | rs786203924 |
openSNP | rs786203924 |
23andMe | rs786203924 |
SNPshot | rs786203924 |
SNPdbe | rs786203924 |
MSV3d | rs786203924 |
GWAS Ctlg | rs786203924 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786203924(-;-) |
Alt | rs786203924(-;-) |
Reference | Rs786203924(TA;TA) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MSH6 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.48028028_48028029delAT |
CLNSRC | |
CLNACC | RCV000167441.2, |