rs876660118
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAAAGCAAGAGAATTTGAGAAGATGA;AAAAGCAAGAGAATTTGAGAAGATGA) | 0 | common in clinvar |
Make rs876660118(-;-) |
Make rs876660118(-;AAAGCAAGAGAATTTGAGAAGATGAA) |
Make rs876660118(AAAGCAAGAGAATTTGAGAAGATGAA;AAAGCAAGAGAATTTGAGAAGATGAA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 47806605 |
Gene | FBXO11, MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs876660118 |
dbSNP (classic) | rs876660118 |
ClinGen | rs876660118 |
ebi | rs876660118 |
HLI | rs876660118 |
Exac | rs876660118 |
Gnomad | rs876660118 |
Varsome | rs876660118 |
LitVar | rs876660118 |
Map | rs876660118 |
PheGenI | rs876660118 |
Biobank | rs876660118 |
1000 genomes | rs876660118 |
hgdp | rs876660118 |
ensembl | rs876660118 |
geneview | rs876660118 |
scholar | rs876660118 |
rs876660118 | |
pharmgkb | rs876660118 |
gwascentral | rs876660118 |
openSNP | rs876660118 |
23andMe | rs876660118 |
SNPshot | rs876660118 |
SNPdbe | rs876660118 |
MSV3d | rs876660118 |
GWAS Ctlg | rs876660118 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876660118(-;-) |
Alt | rs876660118(-;-) |
Reference | Rs876660118(AAAAGCAAGAGAATTTGAGAAGATGA;AAAAGCAAGAGAATTTGAGAAGATGA) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | FBXO11 MSH6 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.48033744_48033769del26 |
CLNSRC | |
CLNACC | RCV000217290.1, |