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rs587777373(-;GCA)

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possible causal congenital heart defect mutation

Is a	genotype
of	rs587777373
Gene	NR2F2, MIR1469
Chromosome	15
Position	96,332,329
mentioned	by

6

Bad

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;GCA)	6	possible causal congenital heart defect mutation

see ClinVar links

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Is a genotype