List of variants in gene LRRK2 reported as uncertain significance by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.3777+7C>T	rs41286480	0.00097
NM_198578.4(LRRK2):c.4536+3A>G	rs41286476	0.00027
NM_198578.4(LRRK2):c.7067C>T (p.Thr2356Ile)	rs113511708	0.00025
NM_198578.4(LRRK2):c.2842C>T (p.Arg948Ter)	rs766809708	0.00001
NM_198578.4(LRRK2):c.5647T>C (p.Phe1883Leu)	rs762890407	0.00001
NM_198578.4(LRRK2):c.1721del (p.Pro574fs)	rs1943372260
NM_198578.4(LRRK2):c.6448G>C (p.Val2150Leu)	rs755564073
NM_198578.4(LRRK2):c.7475G>T (p.Cys2492Phe)	rs774904977

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