List of variants in gene GIPC3 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_133261.3(GIPC3):c.276G>A (p.Leu92=)	rs8113232	0.23935
NM_133261.3(GIPC3):c.593-6C>T	rs10426399	0.21701
NM_133261.3(GIPC3):c.225+11C>T	rs185551765	0.00351
NM_133261.3(GIPC3):c.706-12G>A	rs112949777	0.00222
NM_133261.3(GIPC3):c.856G>A (p.Val286Ile)	rs138339125	0.00126
NM_133261.3(GIPC3):c.906C>T (p.Ala302=)	rs140960269	0.00094
NM_133261.3(GIPC3):c.226-7C>G	rs143968967

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