Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
U4M - |
RCV000003935 | SCV000583862 | pathogenic | Hypercholesterolemia, familial, 1 | 2017-03-30 | criteria provided, single submitter | clinical testing | |
Laboratory for Molecular Medicine, |
RCV000825620 | SCV000966972 | pathogenic | Homozygous familial hypercholesterolemia | 2018-04-06 | criteria provided, single submitter | clinical testing | The p.[Asn564His;Val800_Leu802del] compound allele in LDLR is the most common FH variant in the Netherlands (Kusters 2011) and has been well reported in associa tion with FH in other European populations (Jensen 1997, Castillo 2002, Palacios 2012, ClinVar Variation IDs 226365, 226394, 3737). This compound allele has als o been identified in 2/111690 European chromosomes by the Genome Aggregation Dat abase (gnomAD, http://gnomad.broadinstitute.org; dbSNP rs875989944 and rs3975093 65); however, this frequency is low enough to be consistent with the frequency o f FH in the general population. This compound allele is comprised of two variant s (p.Asn564His in exon 11 and p.Val800_Leu802del in exon 17) on the same copy of the LDLR gene. In vitro functional studies provide some evidence that the p.Asn 564His and p.Val800_Leu802del variants have a synergistic impact on LDLR functio n (Jensen 1997). Although cholesterol levels were significantly elevated in carr iers vs non-carriers (p<0.001; Castillo 2002, Huijgen 2010), the p.[Asn564His;Va l800_Leu802del] compound allele has been reported to lead to relatively mild hyp ercholesterolemia (Castillo 2002, Kusters 2011). Nevertheless, the compound alle le has been associated with increased risk of coronary artery disease (RR 7.83, 95% CI 3.11-19.67; Umans-Echenhausen 2002). In summary, the p.[Asn564His;Val800_ Leu802del] compound allele meets criteria to be classified as pathogenic for fam ilial hypercholesterolemia in an autosomal dominant manner. ACMG/AMP criteria ap plied: PS4, PP1_Strong, PM2, PP3, PS3_Supporting. |
Color Diagnostics, |
RCV001176084 | SCV001339922 | pathogenic | Familial hypercholesterolemia | 2018-12-07 | criteria provided, single submitter | clinical testing | |
Provincial Medical Genetics Program of British Columbia, |
RCV000003935 | SCV002320840 | pathogenic | Hypercholesterolemia, familial, 1 | 2022-01-01 | criteria provided, single submitter | clinical testing | |
OMIM | RCV000003935 | SCV000024100 | pathogenic | Hypercholesterolemia, familial, 1 | 1997-01-01 | no assertion criteria provided | literature only |