List of variants reported as likely benign for Autosomal dominant Parkinson disease 8 by Fulgent Genetics, Fulgent Genetics

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Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.7155A>G (p.Gly2385=)	rs33962975	0.11278
NM_198578.4(LRRK2):c.4624C>T (p.Pro1542Ser)	rs33958906	0.03091
NM_198578.4(LRRK2):c.6844-14_6844-13insA	rs150964683	0.01681
NM_198578.4(LRRK2):c.5509+20A>C	rs11564134	0.01309
NM_198578.4(LRRK2):c.6241A>G (p.Asn2081Asp)	rs33995883	0.01276
NM_198578.4(LRRK2):c.867C>T (p.Asn289=)	rs17490713	0.01182
NM_198578.4(LRRK2):c.3784C>G (p.Pro1262Ala)	rs4640000	0.00717
NM_198578.4(LRRK2):c.5510-9A>G	rs41286460	0.00252
NM_198578.4(LRRK2):c.3333G>T (p.Gln1111His)	rs78365431	0.00121
NM_198578.4(LRRK2):c.1383T>C (p.Ser461=)	rs35847451	0.00047
NM_198578.4(LRRK2):c.2481T>C (p.Ser827=)	rs76890302	0.00038
NM_198578.4(LRRK2):c.7429C>T (p.Arg2477Trp)	rs138780308	0.00035
NM_198578.4(LRRK2):c.1256C>T (p.Ala419Val)	rs34594498	0.00025
NM_198578.4(LRRK2):c.7462+15G>C	rs200420425	0.00025
NM_198578.4(LRRK2):c.2264C>T (p.Pro755Leu)	rs34410987	0.00023
NM_198578.4(LRRK2):c.45T>C (p.Thr15=)	rs142399623	0.00019
NM_198578.4(LRRK2):c.2229T>G (p.Ser743=)	rs200425243	0.00011
NM_198578.4(LRRK2):c.5931C>T (p.His1977=)	rs201119482	0.00003
NM_198578.4(LRRK2):c.2689+19_2689+20dup	rs66810434
NM_198578.4(LRRK2):c.2689+20dup	rs66810434
NM_198578.4(LRRK2):c.4193G>A (p.Arg1398His)	rs7133914
NM_198578.4(LRRK2):c.936G>T (p.Ala312=)	rs41286466

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