Have questions? Visit https://www.reddit.com/r/SNPedia

rs201740483

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201740483(A;G)
Make rs201740483(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position43126647
GeneRET
is asnp
is mentioned by
dbSNPrs201740483
ebirs201740483
HLIrs201740483
Exacrs201740483
Varsomers201740483
Maprs201740483
PheGenIrs201740483
hapmaprs201740483
1000 genomesrs201740483
hgdprs201740483
ensemblrs201740483
gopubmedrs201740483
geneviewrs201740483
scholarrs201740483
googlers201740483
pharmgkbrs201740483
gwascentralrs201740483
openSNPrs201740483
23andMers201740483
23andMe allrs201740483
SNP Nexus

SNPshotrs201740483
SNPdbers201740483
MSV3drs201740483
GWAS Ctlgrs201740483
Max Magnitude0
[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 RCV000123317.3, RCV000163463.1,