"Medizinische Klinik 1/ Institut für Bioinformatik, Universitätsklinik - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 217140	NM_015441.3(OLFML2B):c.2021G>A (p.Gly674Asp)	OLFML2B (G674D +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 217141	NM_015441.3(OLFML2B):c.1606G>A (p.Gly536Ser)	OLFML2B (G536S +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 217139	NM_015441.3(OLFML2B):c.1580G>A (p.Arg527Gln)	OLFML2B (R527Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 217138	NM_015441.3(OLFML2B):c.1544G>A (p.Gly515Glu)	OLFML2B (G515E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 217137	NM_015441.3(OLFML2B):c.1306G>T (p.Ala436Ser)	OLFML2B (A436S +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 217136	NM_015441.3(OLFML2B):c.1058G>A (p.Arg353His)	OLFML2B (R353H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 217135	NM_015441.3(OLFML2B):c.1039C>T (p.Arg347Trp)	OLFML2B (R347W +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 217134	NM_015441.3(OLFML2B):c.44T>G (p.Val15Gly)	OLFML2B (V15G)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic

ClinVar