All of V2483

ID Consequence Gene/Location Detail Geno Type CHD Type
S4879 intron_variant TNF NM_000594.4:c.186+123G>A G/G isolated CHD/non-isoalted CHD: SD/CTDs/LVOTO/RVOTO/APVR/other
S4880 intron_variant TNF NM_000594.4:c.186+123G>A A/G isolated CHD/non-isoalted CHD: SD/CTDs/LVOTO/RVOTO/APVR/other
S4881 intron_variant TNF NM_000594.4:c.186+123G>A A/A isolated CHD/non-isoalted CHD: SD/CTDs/LVOTO/RVOTO/APVR/other
S4882 intron_variant TNF NM_000594.4:c.186+123G>A G isolated CHD/non-isoalted CHD: SD/CTDs/LVOTO/RVOTO/APVR/other
S4883 intron_variant TNF NM_000594.4:c.186+123G>A A isolated CHD/non-isoalted CHD: SD/CTDs/LVOTO/RVOTO/APVR/other

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