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rs2472737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2472737(A;A)
Make rs2472737(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43120057
GeneRET
is asnp
is mentioned by
dbSNPrs2472737
ebirs2472737
HLIrs2472737
Exacrs2472737
Varsomers2472737
Maprs2472737
PheGenIrs2472737
hapmaprs2472737
1000 genomesrs2472737
hgdprs2472737
ensemblrs2472737
gopubmedrs2472737
geneviewrs2472737
scholarrs2472737
googlers2472737
pharmgkbrs2472737
gwascentralrs2472737
openSNPrs2472737
23andMers2472737
23andMe allrs2472737
SNP Nexus

SNPshotrs2472737
SNPdbers2472737
MSV3drs2472737
GWAS Ctlgrs2472737
GMAF0.1873
Max Magnitude0
? (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, RCV000082053.4,



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