List of variants in gene CLN6 reported as not provided by SNPedia

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_017882.3(CLN6):c.446G>A (p.Arg149His)	rs154774638	0.00003
NM_017882.3(CLN6):c.150C>G (p.Tyr50Ter)	rs154774640	0.00002
NM_017882.3(CLN6):c.308G>A (p.Arg103Gln)	rs154774634	0.00002
NM_017882.3(CLN6):c.139C>T (p.Leu47Phe)	rs154774635
NM_017882.3(CLN6):c.17G>C (p.Arg6Thr)	rs154774636
NM_017882.3(CLN6):c.200T>C (p.Leu67Pro)	rs154774633
NM_017882.3(CLN6):c.231C>G (p.Asn77Lys)	rs154774641
NM_017882.3(CLN6):c.712T>A (p.Phe238Ile)	rs154774637
NM_017882.3(CLN6):c.890del (p.Pro297fs)	rs154774639

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