ClinVar Miner

List of variants in gene combination ITGAM, LOC126862332 reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_000632.4(ITGAM):c.739A>G (p.Lys247Glu) rs200610250 0.00010
NM_000632.4(ITGAM):c.706C>T (p.Arg236Ter) rs1030683453 0.00001
NM_000632.4(ITGAM):c.718A>G (p.Asn240Asp) rs778590336 0.00001
NM_000632.4(ITGAM):c.730G>A (p.Gly244Arg) rs748727423 0.00001
NM_000632.4(ITGAM):c.790G>A (p.Asp264Asn) rs761622995 0.00001
NM_000632.4(ITGAM):c.802T>A (p.Tyr268Asn) rs376840611 0.00001
NM_000632.4(ITGAM):c.805G>A (p.Glu269Lys) rs927472766 0.00001
NM_000632.4(ITGAM):c.850G>A (p.Val284Ile) rs749635901 0.00001
NM_000632.4(ITGAM):c.851T>A (p.Val284Asp) rs373307087 0.00001
NM_000632.4(ITGAM):c.705-3C>T
NM_000632.4(ITGAM):c.707G>A (p.Arg236Gln)
NM_000632.4(ITGAM):c.721A>C (p.Ile241Leu) rs889524923
NM_000632.4(ITGAM):c.725C>A (p.Thr242Asn) rs749972434
NM_000632.4(ITGAM):c.745G>A (p.Ala249Thr) rs2079873239
NM_000632.4(ITGAM):c.761T>C (p.Val254Ala) rs2544388039
NM_000632.4(ITGAM):c.770C>T (p.Thr257Met)
NM_000632.4(ITGAM):c.778G>A (p.Glu260Lys) rs2544388111
NM_000632.4(ITGAM):c.803A>T (p.Tyr268Phe) rs776945214
NM_000632.4(ITGAM):c.805G>T (p.Glu269Ter) rs927472766
NM_000632.4(ITGAM):c.808G>A (p.Asp270Asn) rs2144297485
NM_000632.4(ITGAM):c.830G>T (p.Arg277Ile) rs2544388325
NM_000632.4(ITGAM):c.835G>A (p.Gly279Arg) rs2544388363

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