ClinVar Miner

List of variants in gene LRP6 studied for bone disorder

Included ClinVar conditions (1436):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_002336.3(LRP6):c.1004G>T (p.Arg335Leu) rs869320641
NM_002336.3(LRP6):c.1620G>T (p.Leu540Phe) rs869320642
NM_002336.3(LRP6):c.2058C>G (p.Ile686Met) rs869320643
NM_002336.3(LRP6):c.2995G>C (p.Gly999Arg) rs869320644
NM_002336.3(LRP6):c.3365A>C (p.Asp1122Ala) rs869320645
NM_002336.3(LRP6):c.4136G>A (p.Gly1379Asp) rs869320646
NM_002336.3(LRP6):c.4298C>T (p.Ser1433Leu) rs869320647
NM_002336.3(LRP6):c.4593del (p.Cys1532fs) rs869320635

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