Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356611
rs80356611
KCNJ11
0.010 GeneticVariation BEFREE We investigated the functional effects this mutation and another at the same residue (R50P) that led to PNDM in association with developmental delay. 16731833

2006