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rs587777374(A;G)

From SNPedia

possible causal congenital heart defect mutation
Is agenotype
ofrs587777374
GeneNR2F2
Chromosome15
Position96,334,604
mentionedby
Magnitude6
ReputeBad
Geno Mag Summary
(A;G) 6 possible causal congenital heart defect mutation
(G;G) 0 common in clinvar

see ClinVar links