rs1060502886
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TA;TA) | 0 | common in clinvar |
Make rs1060502886(-;-) |
Make rs1060502886(-;TA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 47799798 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs1060502886 |
dbSNP (classic) | rs1060502886 |
ClinGen | rs1060502886 |
ebi | rs1060502886 |
HLI | rs1060502886 |
Exac | rs1060502886 |
Gnomad | rs1060502886 |
Varsome | rs1060502886 |
LitVar | rs1060502886 |
Map | rs1060502886 |
PheGenI | rs1060502886 |
Biobank | rs1060502886 |
1000 genomes | rs1060502886 |
hgdp | rs1060502886 |
ensembl | rs1060502886 |
geneview | rs1060502886 |
scholar | rs1060502886 |
rs1060502886 | |
pharmgkb | rs1060502886 |
gwascentral | rs1060502886 |
openSNP | rs1060502886 |
23andMe | rs1060502886 |
SNPshot | rs1060502886 |
SNPdbe | rs1060502886 |
MSV3d | rs1060502886 |
GWAS Ctlg | rs1060502886 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060502886(-;-) |
Alt | rs1060502886(-;-) |
Reference | Rs1060502886(TA;TA) |
Significance | Pathogenic |
Disease | Lynch syndrome not provided Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MSH6 |
CLNDBN | Lynch syndrome not provided Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.48026937_48026938delTA |
CLNSRC | |
CLNACC | RCV000470844.1, RCV000486089.1, RCV000491721.1, |