List of variants in gene LRP5 reported as pathogenic for perceptual disorders

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002335.4(LRP5):c.211_212del (p.Gln71fs)
NM_002335.4(LRP5):c.2409_2503+79del
NM_002335.4(LRP5):c.2718_2721del (p.Met907fs)	rs1244761864
NM_002335.4(LRP5):c.3085_3086delinsAGGCAGCATCGACAAAACCCAGACAGG (p.Leu1029fs)
NM_002335.4(LRP5):c.3232C>T (p.Arg1078Ter)	rs765402802
NM_002335.4(LRP5):c.4488+2T>G	rs80358322

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