List of variants in gene LRRK2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
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: 30

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HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.6566A>G (p.Tyr2189Cys)	rs35658131	0.00055
NM_198578.4(LRRK2):c.1324C>T (p.His442Tyr)	rs568593066	0.00022
NM_198578.4(LRRK2):c.5822G>A (p.Arg1941His)	rs77428810	0.00022
NM_198578.4(LRRK2):c.3643G>A (p.Ala1215Thr)	rs143710836	0.00012
NM_198578.4(LRRK2):c.2771G>A (p.Arg924His)	rs200795874	0.00008
NM_198578.4(LRRK2):c.309G>C (p.Gln103His)	rs200926937	0.00008
NM_198578.4(LRRK2):c.683G>C (p.Cys228Ser)	rs56108242	0.00008
NM_198578.4(LRRK2):c.546A>G (p.Lys182=)	rs35517158	0.00006
NM_198578.4(LRRK2):c.6928A>G (p.Thr2310Ala)	rs202179802	0.00006
NM_198578.4(LRRK2):c.1874A>G (p.His625Arg)	rs200787476	0.00005
NM_198578.4(LRRK2):c.1546A>G (p.Met516Val)	rs746747483	0.00004
NM_198578.4(LRRK2):c.2758G>A (p.Ala920Thr)	rs201184634	0.00004
NM_198578.4(LRRK2):c.3018A>G (p.Ile1006Met)	rs113217062	0.00004
NM_198578.4(LRRK2):c.3595C>T (p.Arg1199Trp)	rs746433333	0.00004
NM_198578.4(LRRK2):c.137C>T (p.Thr46Met)	rs781394575	0.00003
NM_198578.4(LRRK2):c.1987T>C (p.Ser663Pro)	rs78154388	0.00003
NM_198578.4(LRRK2):c.3091T>C (p.Cys1031Arg)	rs201552816	0.00003
NM_198578.4(LRRK2):c.5870G>T (p.Arg1957Leu)	rs201012950	0.00003
NM_198578.4(LRRK2):c.7382C>T (p.Ala2461Val)	rs201037550	0.00003
NM_198578.4(LRRK2):c.7186_7187dup (p.Val2396_Met2397insTer)	rs281865056	0.00002
NM_198578.4(LRRK2):c.2333G>A (p.Ser778Asn)	rs1356461363	0.00001
NM_198578.4(LRRK2):c.4117G>A (p.Val1373Met)	rs756381499	0.00001
NM_198578.4(LRRK2):c.500T>G (p.Met167Arg)	rs201411683	0.00001
NM_198578.4(LRRK2):c.6220G>A (p.Val2074Ile)	rs200498558	0.00001
NM_198578.4(LRRK2):c.7324C>T (p.Arg2442Cys)	rs199893519	0.00001
NM_198578.4(LRRK2):c.1240G>A (p.Val414Ile)	rs1565682626
NM_198578.4(LRRK2):c.5183G>T (p.Arg1728Leu)	rs145364431
NM_198578.4(LRRK2):c.6187_6191del (p.Leu2062_Leu2063insTer)	rs111739194
NM_198578.4(LRRK2):c.7146A>C (p.Lys2382Asn)	rs919570241
NM_198578.4(LRRK2):c.7430G>A (p.Arg2477Gln)	rs146428335

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