Variants in gene LRP4 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_002334.4(LRP4):c.1048+7G>T	rs148557097	0.00220
NM_002334.4(LRP4):c.639C>T (p.Asp213=)	rs144974139	0.00124
NM_002334.4(LRP4):c.5660C>G (p.Ser1887Cys)	rs149082597	0.00111
NM_002334.4(LRP4):c.3064A>G (p.Asn1022Asp)	rs61742871	0.00098
NM_002334.4(LRP4):c.3620A>G (p.Asn1207Ser)	rs151234321	0.00086
NM_002334.4(LRP4):c.257G>A (p.Arg86His)	rs138239756	0.00083
NM_002334.4(LRP4):c.570C>T (p.Pro190=)	rs147353838	0.00061
NM_002334.4(LRP4):c.1194A>G (p.Glu398=)	rs138589242	0.00058
NM_002334.4(LRP4):c.3944C>T (p.Ser1315Leu)	rs150681693	0.00042
NM_002334.4(LRP4):c.2815-6T>G	rs372210790	0.00030
NM_002334.4(LRP4):c.1654A>T (p.Asn552Tyr)	rs201253200	0.00018
NM_002334.4(LRP4):c.4898C>T (p.Ser1633Leu)	rs146362081	0.00005
NM_002334.4(LRP4):c.2010G>A (p.Thr670=)	rs199654257	0.00001

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