C1853445[trait identifier] AND "Suna and Inan Kirac Foundation Neurode - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1331350	NM_007262.5(PARK7):c.302T>C (p.Leu101Pro)	PARK7 (L101P)	Single nucleotide variant (missense variant)	Autosomal recessive early-onset Parkinson disease 7	GLikely pathogenic
Select item 1334459	NM_007262.5(PARK7):c.322G>A (p.Gly108Ser)	PARK7 (G108S)	Single nucleotide variant (missense variant)	Autosomal recessive early-onset Parkinson disease 7	GPathogenic