Related gene-specific medical variations for Gene (Select 4037) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2549711	NM_002333.4(LRP3):c.472C>G (p.Arg158Gly)	LOC132090548, LRP3 (R158G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1294937	NM_019849.3(SLC7A10):c.*132dup	LRP3, SLC7A10	Duplication (3 prime UTR variant)	not provided	GBenign
Select item 1253365	NM_019849.3(SLC7A10):c.*188C>T	LRP3, SLC7A10	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign

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