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rs2565200

From SNPedia

Orientationminus
Stabilizedminus
Make rs2565200(A;A)
Make rs2565200(A;G)
Make rs2565200(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position43127485
GeneRET
is asnp
is mentioned by
dbSNPrs2565200
ebirs2565200
HLIrs2565200
Exacrs2565200
Varsomers2565200
Maprs2565200
PheGenIrs2565200
hapmaprs2565200
1000 genomesrs2565200
hgdprs2565200
ensemblrs2565200
gopubmedrs2565200
geneviewrs2565200
scholarrs2565200
googlers2565200
pharmgkbrs2565200
gwascentralrs2565200
openSNPrs2565200
23andMers2565200
23andMe allrs2565200
SNP Nexus

SNPshotrs2565200
SNPdbers2565200
MSV3drs2565200
GWAS Ctlgrs2565200
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 24897126OA-icon.png] RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease


[PMID 27798940] Rare RET Variant p.D707E in a Chinese Pedigree with Hereditary Medullary Thyroid Carcinoma.