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rs2506004

From SNPedia

Orientationminus
Stabilizedminus
Make rs2506004(G;G)
Make rs2506004(G;T)
Make rs2506004(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position43086825
GeneRET
is asnp
is mentioned by
dbSNPrs2506004
ebirs2506004
HLIrs2506004
Exacrs2506004
Varsomers2506004
Maprs2506004
PheGenIrs2506004
hapmaprs2506004
1000 genomesrs2506004
hgdprs2506004
ensemblrs2506004
gopubmedrs2506004
geneviewrs2506004
scholarrs2506004
googlers2506004
pharmgkbrs2506004
gwascentralrs2506004
openSNPrs2506004
23andMers2506004
23andMe allrs2506004
SNP Nexus

SNPshotrs2506004
SNPdbers2506004
MSV3drs2506004
GWAS Ctlgrs2506004
GMAF0.2599
Max Magnitude

[PMID 22325379] Intronic RET gene variants in Down syndrome-associated Hirschsprung disease in an African population

[PMID 15759212OA-icon.png] Identifying candidate Hirschsprung disease-associated RET variants.

[PMID 20977903] Variants in RET associated with Hirschsprung's disease affect binding of transcription factors and gene expression.


[PMID 24897126OA-icon.png] RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease


[PMID 24528961] Tissue specific somatic mutations and aganglionosis in Hirschsprung's disease