ClinVar Miner

List of variants in gene PINK1 reported as benign for Parkinson disease

Included ClinVar conditions (41):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_032409.3(PINK1):c.960-5G>A rs3131713 0.83971
NM_032409.3(PINK1):c.388-7A>G rs2298298 0.83839
NM_032409.3(PINK1):c.1018G>A (p.Ala340Thr) rs3738136 0.04637
NM_032409.3(PINK1):c.344A>T (p.Gln115Leu) rs148871409 0.03666
NM_032409.3(PINK1):c.1426G>A (p.Glu476Lys) rs115477764 0.01222
NM_032409.3(PINK1):c.1173T>C (p.Asp391=) rs45499398 0.01177
NM_032409.3(PINK1):c.1502G>A (p.Arg501Gln) rs61744200 0.00956
NM_032409.3(PINK1):c.948C>T (p.Leu316=) rs142183624 0.00363
NM_032409.3(PINK1):c.387+14G>A rs117438827 0.00234
NM_032409.3(PINK1):c.1231G>A (p.Gly411Ser) rs45478900 0.00146
NM_032409.3(PINK1):c.387+20A>G rs368222506 0.00122
NM_032409.3(PINK1):c.936G>A (p.Arg312=) rs56200357 0.00091
NM_032409.3(PINK1):c.558G>C (p.Lys186Asn) rs143204084 0.00055
NM_032409.3(PINK1):c.858G>A (p.Pro286=) rs148144773 0.00019
NM_032409.3(PINK1):c.1362C>T (p.Tyr454=) rs56383368 0.00011
NM_032409.3(PINK1):c.804A>G (p.Leu268=) rs200708848 0.00008
NM_032409.3(PINK1):c.1481C>T (p.Ala494Val) rs542258150 0.00001
NM_032409.3(PINK1):c.1488+14del
NM_032409.3(PINK1):c.827G>A (p.Arg276Gln) rs548506734
NM_032409.3(PINK1):c.88G>C (p.Gly30Arg) rs569753606

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