List of variants in gene 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000213.5(ITGB4):c.513T>C (p.Phe171=)	rs148048907	0.01650
NM_000213.5(ITGB4):c.2963-13G>A	rs77473568	0.00061
NM_000213.5(ITGB4):c.3427A>G (p.Ile1143Val)	rs149481974	0.00056
NM_000213.5(ITGB4):c.1215+19A>G	rs201686414	0.00052
NM_000213.5(ITGB4):c.387C>T (p.Pro129=)	rs140040189	0.00048
NM_000213.5(ITGB4):c.1281G>A (p.Pro427=)	rs150638695	0.00032
NM_000213.5(ITGB4):c.2070C>T (p.Gly690=)	rs140265734	0.00029
NM_000213.5(ITGB4):c.2503C>G (p.Pro835Ala)	rs183705877	0.00029
NM_000213.5(ITGB4):c.2962+9G>C	rs375133413	0.00024
NM_000213.5(ITGB4):c.495C>T (p.Ser165=)	rs75092172	0.00020
NM_000213.5(ITGB4):c.309C>A (p.Pro103=)	rs763268075	0.00019
NM_000213.5(ITGB4):c.2577C>T (p.Ser859=)	rs148787870	0.00018
NM_000213.5(ITGB4):c.1911G>A (p.Ala637=)	rs376183156	0.00003

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