Related gene-specific medical variations for Gene (Select 1604) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3362514	NM_000574.5(CD55):c.148G>A (p.Glu50Lys)	CD55 (E50K)	Single nucleotide variant (missense variant +1 more)	Protein-losing enteropathy	GUncertain significance
Select item 2817394	NM_000574.5(CD55):c.100+18G>A	CD55, LOC129932392	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1642641	NM_000574.5(CD55):c.100+21del	CD55, LOC129932392	Deletion (intron variant)	not provided	GLikely benign
Select item 1641362	NM_000574.5(CD55):c.100+14C>A	CD55, LOC129932392	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1639275	NM_000574.5(CD55):c.100+17C>T	CD55, LOC129932392	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1169262	NM_000574.5(CD55):c.100+14C>T	CD55, LOC129932392	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar