ClinVar Miner

List of variants in gene VLDLR reported as likely benign for congenital nervous system disorder

Included ClinVar conditions (854):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_003383.5(VLDLR):c.*551T>C rs8210 0.16040
NM_003383.5(VLDLR):c.1187-3C>T rs11789583 0.15129
NM_003383.5(VLDLR):c.2067A>G (p.Gln689=) rs6148 0.13882
NM_003383.5(VLDLR):c.175G>A (p.Val59Ile) rs6149 0.05632
NM_003383.5(VLDLR):c.944-5T>C rs35782329 0.03136
NM_003383.5(VLDLR):c.468C>T (p.Pro156=) rs2242105 0.00058

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