List of variants in gene CLN8 reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_018941.4(CLN8):c.-123-127C>T	rs4875957	0.81090
NM_018941.4(CLN8):c.544-227A>G	rs3935479	0.07779
NM_018941.4(CLN8):c.544-124T>C	rs12546965	0.07202
NM_018941.4(CLN8):c.-124+113G>A	rs373818270	0.01856
NM_018941.4(CLN8):c.685C>G (p.Pro229Ala)	rs150047904	0.00893
NM_018941.4(CLN8):c.777T>C (p.Asn259=)	rs34814682	0.00334
NM_018941.4(CLN8):c.290G>A (p.Arg97His)	rs116605307	0.00236
NM_018941.4(CLN8):c.-129G>T	rs1024120201	0.00064
NM_018941.4(CLN8):c.111C>T (p.Gly37=)	rs753430388	0.00002
NM_018941.4(CLN8):c.-108G>A	rs1048152901
NM_018941.4(CLN8):c.-123-225G>C	rs4875806

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