ClinVar Miner

List of variants in gene LRP5 reported as benign for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_002335.4(LRP5):c.1015+15C>T rs201268200 0.11677
NM_002335.4(LRP5):c.3989C>T (p.Ala1330Val) rs3736228 0.10701
NM_002335.4(LRP5):c.1999G>A (p.Val667Met) rs4988321 0.03472
NM_002335.4(LRP5):c.687-17C>T rs186410639 0.00751
NM_002335.4(LRP5):c.2544G>A (p.Pro848=) rs148271293 0.00083

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