RS2435357 RET

Health Risk Chr 10:43086608
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What This Variant Does
"This SNP, located in the first intron of the RET gene, has been associated with Hirschsprung disease...
Associated Conditions
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Hirschsprung disease OR: 23.12 3E-21 PubMed
Other Variants in RET
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