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rs587777372(A;T)

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possible congenital heart defect mutation

Is a	genotype
of	rs587777372
Gene	NR2F2
Chromosome	15
Position	96,334,247
mentioned	by

6

Bad

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;T)	6	possible congenital heart defect mutation

see ClinVar links

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Is a genotype