CHDRFKB

ID	Consequence	Gene/Location	Detail	Geno Type	CHD Type
S2925	intron_variant	FIGN	NC_000002.12:g.163641436C>G	C/G+G/G	NA: Septa and valve abnormalities
S2926	intron_variant	FIGN	NC_000002.12:g.163641436C>G	C/C+G/G	NA: Septa and valve abnormalities