rs786205215
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs786205215(C;T) |
Make rs786205215(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 58363582 |
Gene | RNF43 |
is a | snp |
is | mentioned by |
dbSNP | rs786205215 |
dbSNP (classic) | rs786205215 |
ClinGen | rs786205215 |
ebi | rs786205215 |
HLI | rs786205215 |
Exac | rs786205215 |
Gnomad | rs786205215 |
Varsome | rs786205215 |
LitVar | rs786205215 |
Map | rs786205215 |
PheGenI | rs786205215 |
Biobank | rs786205215 |
1000 genomes | rs786205215 |
hgdp | rs786205215 |
ensembl | rs786205215 |
geneview | rs786205215 |
scholar | rs786205215 |
rs786205215 | |
pharmgkb | rs786205215 |
gwascentral | rs786205215 |
openSNP | rs786205215 |
23andMe | rs786205215 |
SNPshot | rs786205215 |
SNPdbe | rs786205215 |
MSV3d | rs786205215 |
GWAS Ctlg | rs786205215 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205215(T;T) |
Alt | rs786205215(T;T) |
Reference | Rs786205215(C;C) |
Significance | Pathogenic |
Disease | Colon Serrated Polyposis Sessile serrated polyposis cancer syndrome |
Variation | info |
Gene | RNF43 |
CLNDBN | Colon Serrated Polyposis Sessile serrated polyposis cancer syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.56440943G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000170445.1, RCV000240616.1, |