List of variants in gene GPC3 reported as benign for not specified

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004484.4(GPC3):c.1500T>C (p.Asp500=)	rs2314298	0.06746
NM_004484.4(GPC3):c.1626A>G (p.Ala542=)	rs61754631	0.05751
NM_004484.4(GPC3):c.-39G>A	rs185369906	0.01235
NM_004484.4(GPC3):c.204G>A (p.Lys68=)	rs61754632	0.01163
NM_004484.4(GPC3):c.1285G>A (p.Val429Met)	rs11539789	0.00333
NM_004484.4(GPC3):c.1167-8T>C	rs182950534	0.00303
NM_004484.4(GPC3):c.995A>G (p.Gln332Arg)	rs78696048	0.00065
NM_004484.4(GPC3):c.168C>G (p.Pro56=)	rs188592483	0.00005
NM_004484.4(GPC3):c.1033-4250del	rs372010975
NM_004484.4(GPC3):c.1033-4262dup	rs372010975
NM_004484.4(GPC3):c.338-20dup	rs370737647
NM_004484.4(GPC3):c.338-5del	rs370737647

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