rs1060502882
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1060502882(-;-) |
Make rs1060502882(-;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 47801132 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs1060502882 |
dbSNP (classic) | rs1060502882 |
ClinGen | rs1060502882 |
ebi | rs1060502882 |
HLI | rs1060502882 |
Exac | rs1060502882 |
Gnomad | rs1060502882 |
Varsome | rs1060502882 |
LitVar | rs1060502882 |
Map | rs1060502882 |
PheGenI | rs1060502882 |
Biobank | rs1060502882 |
1000 genomes | rs1060502882 |
hgdp | rs1060502882 |
ensembl | rs1060502882 |
geneview | rs1060502882 |
scholar | rs1060502882 |
rs1060502882 | |
pharmgkb | rs1060502882 |
gwascentral | rs1060502882 |
openSNP | rs1060502882 |
23andMe | rs1060502882 |
SNPshot | rs1060502882 |
SNPdbe | rs1060502882 |
MSV3d | rs1060502882 |
GWAS Ctlg | rs1060502882 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060502882(-;-) |
Alt | rs1060502882(-;-) |
Reference | Rs1060502882(C;C) |
Significance | Pathogenic |
Disease | Lynch syndrome |
Variation | info |
Gene | MSH6 |
CLNDBN | Lynch syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.48028271delC |
CLNSRC | |
CLNACC | RCV000473512.1, |