ClinVar Miner

List of variants in gene combination LOC130007688, LRRK2 reported as uncertain significance for Autosomal dominant Parkinson disease 8

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.-74C>A	rs1422910994	0.00004
NM_198578.4(LRRK2):c.-91C>T	rs957511525

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