rs483352717
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs483352717(A;A) |
Make rs483352717(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 41225561 |
Gene | CTNNB1 |
is a | snp |
is | mentioned by |
dbSNP | rs483352717 |
dbSNP (classic) | rs483352717 |
ClinGen | rs483352717 |
ebi | rs483352717 |
HLI | rs483352717 |
Exac | rs483352717 |
Gnomad | rs483352717 |
Varsome | rs483352717 |
LitVar | rs483352717 |
Map | rs483352717 |
PheGenI | rs483352717 |
Biobank | rs483352717 |
1000 genomes | rs483352717 |
hgdp | rs483352717 |
ensembl | rs483352717 |
geneview | rs483352717 |
scholar | rs483352717 |
rs483352717 | |
pharmgkb | rs483352717 |
gwascentral | rs483352717 |
openSNP | rs483352717 |
23andMe | rs483352717 |
SNPshot | rs483352717 |
SNPdbe | rs483352717 |
MSV3d | rs483352717 |
GWAS Ctlg | rs483352717 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs483352717(A;A) |
Alt | rs483352717(A;A) |
Reference | Rs483352717(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CTNNB1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.41267052G>A |
CLNSRC | |
CLNACC | RCV000087198.2, |