rs876658296
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GGCCCAGGCCCTT;GGCCCAGGCCCTT) | 0 | common in clinvar |
Make rs876658296(-;-) |
Make rs876658296(-;CCAGGCCCTTGGC) |
Make rs876658296(CCAGGCCCTTGGC;CCAGGCCCTTGGC) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 47783403 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs876658296 |
dbSNP (classic) | rs876658296 |
ClinGen | rs876658296 |
ebi | rs876658296 |
HLI | rs876658296 |
Exac | rs876658296 |
Gnomad | rs876658296 |
Varsome | rs876658296 |
LitVar | rs876658296 |
Map | rs876658296 |
PheGenI | rs876658296 |
Biobank | rs876658296 |
1000 genomes | rs876658296 |
hgdp | rs876658296 |
ensembl | rs876658296 |
geneview | rs876658296 |
scholar | rs876658296 |
rs876658296 | |
pharmgkb | rs876658296 |
gwascentral | rs876658296 |
openSNP | rs876658296 |
23andMe | rs876658296 |
SNPshot | rs876658296 |
SNPdbe | rs876658296 |
MSV3d | rs876658296 |
GWAS Ctlg | rs876658296 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876658296(-;-) |
Alt | rs876658296(-;-) |
Reference | Rs876658296(GGCCCAGGCCCTT;GGCCCAGGCCCTT) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MSH6 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.48010542_48010554delCCAGGCCCTTGGC |
CLNSRC | |
CLNACC | RCV000215541.1, |