ClinVar Miner

List of variants studied for Parkinson disease 18, autosomal dominant, susceptibility to by Neuberg Centre For Genomic Medicine, NCGM

Included ClinVar conditions (1):

Parkinson disease 18, autosomal dominant, susceptibility to

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_198241.3(EIF4G1):c.1657A>G (p.Asn553Asp)	rs2474067302
NM_198241.3(EIF4G1):c.3775A>T (p.Met1259Leu)	rs753764322
NM_198241.3(EIF4G1):c.956C>G (p.Pro319Arg)	rs1209748965

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