Variants in gene LRRK2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_198578.3(LRRK2):c.149A>G (p.His50Arg)	rs2256408	0.03048
NM_198578.4(LRRK2):c.5163A>G (p.Ser1721=)	rs79909111	0.00293
NM_198578.4(LRRK2):c.1000G>A (p.Glu334Lys)	rs78501232	0.00266
NM_198578.4(LRRK2):c.225G>A (p.Ala75=)	rs75054132	0.00146
NM_198578.4(LRRK2):c.3777+7C>T	rs41286480	0.00097
NM_198578.4(LRRK2):c.2378G>T (p.Arg793Met)	rs35173587	0.00085
NM_198578.4(LRRK2):c.347+2T>C	rs141221000	0.00084
NM_198578.4(LRRK2):c.7153G>A (p.Gly2385Arg)	rs34778348	0.00058
NM_198578.4(LRRK2):c.825T>C (p.His275=)	rs72546315	0.00041
NM_198578.4(LRRK2):c.1561A>G (p.Arg521Gly)	rs35328937	0.00016
NM_198578.4(LRRK2):c.6929C>T (p.Thr2310Met)	rs200002022	0.00004
NM_198578.4(LRRK2):c.6281-3dup	rs780258764

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