rs2472737

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs2472737(A;A)

Make rs2472737(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43120057

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs2472737
dbSNP (classic)	rs2472737
ClinGen	rs2472737
ebi	rs2472737
HLI	rs2472737
Exac	rs2472737
Gnomad	rs2472737
Varsome	rs2472737
LitVar	rs2472737
Map	rs2472737
PheGenI	rs2472737
Biobank	rs2472737
1000 genomes	rs2472737
hgdp	rs2472737
ensembl	rs2472737
geneview	rs2472737
scholar	rs2472737
google	rs2472737
pharmgkb	rs2472737
gwascentral	rs2472737
openSNP	rs2472737
23andMe	rs2472737
SNPshot	rs2472737
SNPdbe	rs2472737
MSV3d	rs2472737
GWAS Ctlg	rs2472737

GMAF

0.1873

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 16118333] Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?

ClinVar
Risk	rs2472737(A;A)
Alt	rs2472737(A;A)
Reference	Rs2472737(G;G)
Significance	Non-pathogenic
Disease	No MEN2 disease not specified
Variation	info
Gene	RET
CLNDBN	No MEN2 disease not specified
Reversed	0
HGVS	NC_000010.10:g.43615505G>A
CLNSRC	ClinVar
CLNACC	RCV000021870.1, RCV000082053.5,

[PMID 11302967] Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.