List of variants in gene ITGB2 reported as likely benign for not provided

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000211.5(ITGB2):c.1756C>T (p.Arg586Trp)	rs5030672	0.00847
NM_000211.5(ITGB2):c.1888G>A (p.Glu630Lys)	rs2230531	0.00539
NM_000211.5(ITGB2):c.147+9C>T	rs199948899	0.00243
NM_000211.5(ITGB2):c.1635C>T (p.Asn545=)	rs61747606	0.00224
NM_000211.5(ITGB2):c.162G>A (p.Pro54=)	rs138303556	0.00201
NM_000211.5(ITGB2):c.453C>T (p.Gly151=)	rs372501675	0.00021
NM_000211.5(ITGB2):c.150C>T (p.Asn50=)	rs1601316617
NM_000211.5(ITGB2):c.1944G>A (p.Pro648=)	rs139840790
NM_000211.5(ITGB2):c.2292C>T (p.Pro764=)	rs1350166836

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