ClinVar Miner

List of variants reported as benign for Parkinson disease by Invitae

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_000345.4(SNCA):c.408C>T (p.Tyr136=) rs76642636
NM_001256864.2(DNAJC6):c.1456C>T (p.Leu486Phe) rs78141380
NM_001256864.2(DNAJC6):c.678G>A (p.Ala226=) rs61753391
NM_001256864.2(DNAJC6):c.745A>G (p.Ile249Val) rs149588872
NM_001256864.2(DNAJC6):c.996-9T>C rs187965193
NM_003895.3(SYNJ1):c.1236-8G>T rs138882423
NM_003895.3(SYNJ1):c.123G>A (p.Ala41=) rs61750221
NM_003895.3(SYNJ1):c.160C>T (p.Pro54Ser) rs61755328
NM_003895.3(SYNJ1):c.1663G>A (p.Val555Ile) rs113708828
NM_003895.3(SYNJ1):c.2031G>A (p.Leu677=) rs534908601
NM_003895.3(SYNJ1):c.2343T>A (p.Val781=) rs566533509
NM_003895.3(SYNJ1):c.3060G>T (p.Met1020Ile) rs115683257
NM_003895.3(SYNJ1):c.3486A>G (p.Pro1162=) rs368850131
NM_003895.3(SYNJ1):c.4032+5G>T rs61750220
NM_003895.3(SYNJ1):c.4215_4216insAATAC (p.Leu1406fs) rs869265580
NM_003895.3(SYNJ1):c.4344G>A (p.Arg1448=) rs145347648
NM_003895.3(SYNJ1):c.4358G>A (p.Gly1453Glu) rs61750217
NM_003895.3(SYNJ1):c.4640C>T (p.Pro1547Leu) rs76056543
NM_003895.3(SYNJ1):c.596+9A>G rs76502784
NM_003895.3(SYNJ1):c.690A>G (p.Thr230=) rs61756694
NM_003895.3(SYNJ1):c.822+7A>G rs187016397
NM_003895.3(SYNJ1):c.823-15dup rs202044634
NM_004562.3(PRKN):c.101A>G (p.Gln34Arg) rs148851677
NM_004562.3(PRKN):c.111G>A (p.Pro37=) rs77795533
NM_004562.3(PRKN):c.1180G>A (p.Asp394Asn) rs1801334
NM_004562.3(PRKN):c.1204C>T (p.Arg402Cys) rs55830907
NM_004562.3(PRKN):c.136G>A (p.Ala46Thr) rs75860381
NM_004562.3(PRKN):c.245C>A (p.Ala82Glu) rs55774500
NM_004562.3(PRKN):c.458C>G (p.Pro153Arg) rs55654276
NM_004562.3(PRKN):c.574A>C (p.Met192Leu) rs9456735
NM_004562.3(PRKN):c.783A>G (p.Leu261=) rs9456711
NM_004562.3(PRKN):c.816C>T (p.Leu272=) rs143902760
NM_004562.3(PRKN):c.957T>C (p.Gly319=) rs144340740
NM_007262.5(PARK7):c.234C>T (p.Gly78=) rs11548937
NM_007262.5(PARK7):c.293G>A (p.Arg98Gln) rs71653619
NM_012179.4(FBXO7):c.1144+9C>T rs199954341
NM_012179.4(FBXO7):c.540A>G (p.Pro180=) rs41311141
NM_012179.4(FBXO7):c.693C>T (p.Ser231=) rs61752254
NM_018206.6(VPS35):c.1938= (p.His646=) rs168745
NM_022089.4(ATP13A2):c.1005C>T (p.Ala335=) rs56290406
NM_022089.4(ATP13A2):c.1128C>T (p.Cys376=) rs148970081
NM_022089.4(ATP13A2):c.1195+10G>A rs55689004
NM_022089.4(ATP13A2):c.1195+9C>T rs117758987
NM_022089.4(ATP13A2):c.132A>G (p.Pro44=) rs200816691
NM_022089.4(ATP13A2):c.1614C>T (p.Pro538=) rs56351817
NM_022089.4(ATP13A2):c.1617G>T (p.Leu539=) rs61739752
NM_022089.4(ATP13A2):c.2093T>C (p.Val698Ala) rs61734958
NM_022089.4(ATP13A2):c.2367C>T (p.Leu789=) rs140048110
NM_022089.4(ATP13A2):c.2724G>A (p.Ser908=) rs79724242
NM_022089.4(ATP13A2):c.3144C>G (p.Thr1048=) rs56126202
NM_022089.4(ATP13A2):c.453C>T (p.Ser151=) rs55979991
NM_022089.4(ATP13A2):c.881G>A (p.Arg294Gln) rs56367069
NM_032409.3(PINK1):c.1173T>C (p.Asp391=) rs45499398
NM_032409.3(PINK1):c.804A>G (p.Leu268=) rs200708848
NM_032409.3(PINK1):c.858G>A (p.Pro286=) rs148144773
NM_198578.3(LRRK2):c.149A>G (p.His50Arg) rs2256408
NM_198578.4(LRRK2):c.1182-4A>G rs7135747
NM_198578.4(LRRK2):c.3333G>T (p.Gln1111His) rs78365431
NM_198578.4(LRRK2):c.3778-9C>T rs114948984
NM_198578.4(LRRK2):c.4541G>A (p.Arg1514Gln) rs35507033
NM_198578.4(LRRK2):c.4624C>T (p.Pro1542Ser) rs33958906
NM_198578.4(LRRK2):c.4937T>C (p.Met1646Thr) rs35303786
NM_198578.4(LRRK2):c.6241A>G (p.Asn2081Asp) rs33995883
NM_198578.4(LRRK2):c.867C>T (p.Asn289=) rs17490713

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