List of variants reported as pathogenic for Parkinson disease, late-onset by Fulgent Genetics, Fulgent Genetics

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000157.4(GBA1):c.1226A>G (p.Asn409Ser)	rs76763715	0.00191
NM_198578.4(LRRK2):c.6055G>A (p.Gly2019Ser)	rs34637584	0.00036
NM_000157.4(GBA1):c.1342G>C (p.Asp448His)	rs1064651	0.00020
NM_000157.4(GBA1):c.115+1G>A	rs104886460	0.00006
NM_000157.4(GBA1):c.1504C>T (p.Arg502Cys)	rs80356771	0.00006
NM_000157.4(GBA1):c.1604G>A (p.Arg535His)	rs75822236	0.00006
NM_000157.4(GBA1):c.887G>A (p.Arg296Gln)	rs78973108	0.00004
NM_000157.4(GBA1):c.1297G>T (p.Val433Leu)	rs80356769	0.00001
NM_000157.4(GBA1):c.604C>T (p.Arg202Ter)	rs1009850780	0.00001
NM_000157.4(GBA1):c.635C>G (p.Ser212Ter)	rs1671872221
NM_000157.4(GBA1):c.653G>A (p.Trp218Ter)	rs867929413
NM_001005741.2(GBA1):c.[1448T>C;1483G>C;1497G>C]

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