List of variants in gene PINK1 reported as uncertain significance by Athena Diagnostics Inc

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_032409.3(PINK1):c.67G>A (p.Gly23Ser)	rs551542832	0.00125
NM_032409.3(PINK1):c.952A>T (p.Met318Leu)	rs139226733	0.00093
NM_032409.3(PINK1):c.851C>A (p.Ser284Tyr)	rs113092523	0.00056
NM_032409.3(PINK1):c.776+38_776+40del	rs760722267	0.00031
NM_032409.3(PINK1):c.1382T>G (p.Leu461Arg)	rs144440543	0.00006
NM_032409.3(PINK1):c.434C>T (p.Thr145Met)	rs45604240	0.00002
NM_032409.3(PINK1):c.935G>A (p.Arg312Gln)	rs202128685	0.00002
NM_032409.3(PINK1):c.1108G>A (p.Val370Met)	rs1570405073
NM_032409.3(PINK1):c.1183G>A (p.Gly395Ser)

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