List of variants in gene combination GALK1, ITGB4 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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_000213.5(ITGB4):c.5248G>A (p.Gly1750Arg)	rs151327791	0.00173
NM_000213.5(ITGB4):c.5091C>T (p.Pro1697=)	rs150804109	0.00068
NM_000213.5(ITGB4):c.5307C>T (p.Ser1769=)	rs145897252	0.00018
NM_000213.5(ITGB4):c.4857A>G (p.Glu1619=)	rs369462022	0.00006
NM_000213.5(ITGB4):c.4932A>G (p.Pro1644=)	rs368991974	0.00004
NM_000213.5(ITGB4):c.5121C>T (p.Ser1707=)	rs201439404	0.00001
NM_000213.5(ITGB4):c.3885C>T (p.Arg1295=)	rs375483568

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