rs201740483

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
google	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,