rs201740483
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs201740483(A;G) |
Make rs201740483(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 43126647 |
Gene | RET |
is a | snp |
is | mentioned by |
dbSNP | rs201740483 |
dbSNP (classic) | rs201740483 |
ClinGen | rs201740483 |
ebi | rs201740483 |
HLI | rs201740483 |
Exac | rs201740483 |
Gnomad | rs201740483 |
Varsome | rs201740483 |
LitVar | rs201740483 |
Map | rs201740483 |
PheGenI | rs201740483 |
Biobank | rs201740483 |
1000 genomes | rs201740483 |
hgdp | rs201740483 |
ensembl | rs201740483 |
geneview | rs201740483 |
scholar | rs201740483 |
rs201740483 | |
pharmgkb | rs201740483 |
gwascentral | rs201740483 |
openSNP | rs201740483 |
23andMe | rs201740483 |
SNPshot | rs201740483 |
SNPdbe | rs201740483 |
MSV3d | rs201740483 |
GWAS Ctlg | rs201740483 |
Max Magnitude | 0 |
[PMID 27120077] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.
ClinVar | |
---|---|
Risk | rs201740483(G;G) |
Alt | rs201740483(G;G) |
Reference | Rs201740483(A;A) |
Significance | Probable-non-pathogenic |
Disease | Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RET |
CLNDBN | Multiple endocrine neoplasia, type 2 Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.43622095A>G |
CLNSRC | |
CLNACC | RCV000123317.4, RCV000163463.2, |