List of variants in gene LDLRAP1 reported as likely benign for Familial hypercholesterolemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_015627.3(LDLRAP1):c.653C>T (p.Thr218Ile)	rs114583297	0.00817
NM_015627.3(LDLRAP1):c.672C>T (p.Ser224=)	rs41291054	0.00191
NM_015627.3(LDLRAP1):c.396C>T (p.Ile132=)	rs369497122	0.00054
NM_015627.3(LDLRAP1):c.141G>A (p.Leu47=)	rs543454612	0.00009
NM_015627.3(LDLRAP1):c.114G>C (p.Thr38=)	rs138908999	0.00006
NM_015627.3(LDLRAP1):c.573C>T (p.Asp191=)	rs375358854	0.00006
NM_015627.3(LDLRAP1):c.861C>T (p.Leu287=)	rs767867837	0.00006
NM_015627.3(LDLRAP1):c.621C>T (p.Val207=)	rs554028072	0.00003
NM_015627.3(LDLRAP1):c.645A>G (p.Leu215=)	rs776681796	0.00002
NM_015627.3(LDLRAP1):c.617-8C>T	rs746302717	0.00001
NM_015627.3(LDLRAP1):c.363A>G (p.Ala121=)	rs1572039510

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