C4551957[trait identifier] AND "Mayo Clinic Laboratories, Mayo Clinic" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 547863	NM_005045.4(RELN):c.7757C>T (p.Thr2586Ile)	RELN (T2586I)	Single nucleotide variant (missense variant)	Norman-Roberts syndrome +4 more	GUncertain significance
Select item 95226	NM_005045.4(RELN):c.6647G>A (p.Arg2216Gln)	RELN (R2216Q)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 281632	NM_005045.4(RELN):c.5822T>C (p.Val1941Ala)	RELN (V1941A)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 95223	NM_005045.4(RELN):c.5711C>T (p.Thr1904Met)	RELN (T1904M)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 542574	NM_005045.4(RELN):c.1336G>C (p.Glu446Gln)	LOC126860131, RELN (E446Q)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 547865	NM_005097.4(LGI1):c.407G>A (p.Arg136Gln)	LGI1 (R136Q)	Single nucleotide variant (missense variant +1 more)	Epilepsy, familial temporal lobe, 1 +1 more	GUncertain significance

ClinVar