rs182024561
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs182024561(C;T) |
Make rs182024561(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 47805662 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs182024561 |
dbSNP (classic) | rs182024561 |
ClinGen | rs182024561 |
ebi | rs182024561 |
HLI | rs182024561 |
Exac | rs182024561 |
Gnomad | rs182024561 |
Varsome | rs182024561 |
LitVar | rs182024561 |
Map | rs182024561 |
PheGenI | rs182024561 |
Biobank | rs182024561 |
1000 genomes | rs182024561 |
hgdp | rs182024561 |
ensembl | rs182024561 |
geneview | rs182024561 |
scholar | rs182024561 |
rs182024561 | |
pharmgkb | rs182024561 |
gwascentral | rs182024561 |
openSNP | rs182024561 |
23andMe | rs182024561 |
SNPshot | rs182024561 |
SNPdbe | rs182024561 |
MSV3d | rs182024561 |
GWAS Ctlg | rs182024561 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs182024561(G;G) rs182024561(T;T) |
Alt | rs182024561(G;G) rs182024561(T;T) |
Reference | Rs182024561(C;C) |
Significance | Probable-Pathogenic |
Disease | Lynch syndrome Hereditary cancer-predisposing syndrome not specified |
Variation | info |
Gene | MSH6 |
CLNDBN | Lynch syndrome Hereditary cancer-predisposing syndrome not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.48032801C>G; NC_000002.11:g.48032801C>T |
CLNSRC | |
CLNACC | RCV000074891.2, RCV000220560.2, RCV000483164.1, RCV000220632.1, |