All of V1386

ID Consequence Gene/Location Detail Geno Type CHD Type
S2859 missense_variant GATA4 NM_001308093.1:c.1138G>A A non-isolated CHD: TOF, PFO
S2861 missense_variant GATA4 NM_001308093.1:c.1138G>A A non-isolated CHD: TOF, PFO

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