rs551060742
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs551060742(C;T) |
Make rs551060742(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 47482929 |
Gene | MSH2 |
is a | snp |
is | mentioned by |
dbSNP | rs551060742 |
dbSNP (classic) | rs551060742 |
ClinGen | rs551060742 |
ebi | rs551060742 |
HLI | rs551060742 |
Exac | rs551060742 |
Gnomad | rs551060742 |
Varsome | rs551060742 |
LitVar | rs551060742 |
Map | rs551060742 |
PheGenI | rs551060742 |
Biobank | rs551060742 |
1000 genomes | rs551060742 |
hgdp | rs551060742 |
ensembl | rs551060742 |
geneview | rs551060742 |
scholar | rs551060742 |
rs551060742 | |
pharmgkb | rs551060742 |
gwascentral | rs551060742 |
openSNP | rs551060742 |
23andMe | rs551060742 |
SNPshot | rs551060742 |
SNPdbe | rs551060742 |
MSV3d | rs551060742 |
GWAS Ctlg | rs551060742 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs551060742(T;T) |
Alt | rs551060742(T;T) |
Reference | Rs551060742(C;C) |
Significance | Probable-non-pathogenic |
Disease | Lynch syndrome not specified Lynch syndrome I Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MSH2 |
CLNDBN | Lynch syndrome not specified Lynch syndrome I Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.47710068C>T |
CLNSRC | International Society for Gastrointestinal Hereditary Tumours |
CLNACC | RCV000076547.3, RCV000236645.2, RCV000410460.1, RCV000487485.1, |