Related gene-specific medical variations for Gene (Select 79174) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3269486	NM_024324.5(CRELD2):c.884C>T (p.Ser295Leu)	CRELD2, LOC130067777 (S267L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2561200	NM_024324.5(CRELD2):c.13C>T (p.Arg5Cys)	CRELD2, LOC130067776 (R5C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398510	NM_024324.5(CRELD2):c.916G>A (p.Glu306Lys)	CRELD2, LOC130067777 (E274K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347282	NM_024324.5(CRELD2):c.65C>T (p.Pro22Leu)	CRELD2, LOC130067776 (P22L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264416	NM_024324.5(CRELD2):c.944A>G (p.Tyr315Cys)	CRELD2, LOC130067777 (Y287C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207533	NM_024324.5(CRELD2):c.40C>T (p.Leu14Phe)	CRELD2, LOC130067776 (L14F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 777313	NM_024324.5(CRELD2):c.882C>T (p.Cys294=)	CRELD2, LOC130067777	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign

ClinVar