"Eurofins Ntd Llc (ga)"[submitter] AND "LOC126860130"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95239	NM_005045.4(RELN):c.9763+3C>G	LOC126860130, RELN +1 more	Single nucleotide variant (intron variant)	not provided +2 more	GUncertain significance
Select item 290106	NM_005045.4(RELN):c.9750C>T (p.Asp3250=)	LOC126860130, RELN +1 more	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 497424	NM_005045.4(RELN):c.9725C>T (p.Thr3242Met)	LOC126860130, RELN +1 more (T3242M)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 167575	NM_005045.4(RELN):c.9690T>G (p.Ala3230=)	LOC126860130, RELN +1 more	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 498861	NM_005045.4(RELN):c.9673G>A (p.Val3225Met)	LOC126860130, RELN +1 more (V3225M)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 598368	NM_005045.4(RELN):c.9620G>A (p.Arg3207His)	LOC126860130, RELN +1 more (R3207H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 498490	NM_005045.4(RELN):c.9605+6T>A	LOC126860130, RELN +1 more	Single nucleotide variant (intron variant)	not provided +2 more	GUncertain significance

ClinVar