"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LRP12"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2658740	NM_013437.5(LRP12):c.2515G>A (p.Asp839Asn)	LRP12 (D820N +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2658741	NM_013437.5(LRP12):c.2482C>T (p.Arg828Cys)	LRP12 (R809C +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3067250	NM_013437.5(LRP12):c.2384T>C (p.Leu795Pro)	LRP12 (L776P +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2515261	NM_013437.5(LRP12):c.2194C>T (p.Arg732Cys)	LRP12 (R713C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2673157	NM_013437.5(LRP12):c.1887C>T (p.Val629=)	LRP12	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1335717	NM_013437.5(LRP12):c.1080T>C (p.Asn360=)	LRP12	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2658742	NM_013437.5(LRP12):c.1063T>G (p.Cys355Gly)	LRP12 (C336G +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3234238	NM_013437.5(LRP12):c.519T>C (p.Cys173=)	LRP12	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3239320	NM_013437.5(LRP12):c.42G>T (p.Arg14Ser)	LRP12 (R14S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar