List of variants in gene LDLRAP1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_015627.3(LDLRAP1):c.712C>T (p.Arg238Trp)	rs41291058	0.03285
NM_015627.3(LDLRAP1):c.*766dup	rs149951294	0.03084
NM_015627.3(LDLRAP1):c.*1222T>C	rs76969561	0.02186
NM_015627.3(LDLRAP1):c.*1115C>T	rs41307931	0.00254
NM_015627.3(LDLRAP1):c.*238C>T	rs114902249	0.00237
NM_015627.3(LDLRAP1):c.*506C>T	rs148168078	0.00197
NM_015627.3(LDLRAP1):c.*1711G>A	rs41312264	0.00053
NM_015627.3(LDLRAP1):c.*803C>T	rs371833162	0.00009
NM_015627.3(LDLRAP1):c.861C>T (p.Leu287=)	rs767867837	0.00006

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