ClinVar Miner

List of variants reported as likely pathogenic for adult neuronal ceroid lipofuscinosis by Neuberg Centre For Genomic Medicine, NCGM

Included ClinVar conditions (9):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_017882.3(CLN6):c.662A>C (p.Tyr221Ser)	rs764571295	0.00003
NM_017882.3(CLN6):c.775G>A (p.Gly259Ser)	rs150363441	0.00002

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