ClinVar Miner

List of variants in gene FREM2 reported as uncertain significance by GeneDx

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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_207361.6(FREM2):c.2128C>T (p.Arg710Cys) rs41292753 0.00274
NM_207361.6(FREM2):c.9038C>T (p.Thr3013Met) rs114400765 0.00118
NM_207361.6(FREM2):c.7429C>T (p.Arg2477Trp) rs143571375 0.00115
NM_207361.6(FREM2):c.3539C>G (p.Pro1180Arg) rs139236965 0.00107
NM_207361.6(FREM2):c.1580C>T (p.Ser527Leu) rs139804851 0.00084
NM_207361.6(FREM2):c.6664C>T (p.Pro2222Ser) rs137899618 0.00050
NM_207361.6(FREM2):c.181G>C (p.Ala61Pro) rs553605556 0.00032
NM_207361.6(FREM2):c.2432G>A (p.Gly811Glu) rs147293913 0.00031
NM_207361.6(FREM2):c.4558C>T (p.Arg1520Trp) rs142322683 0.00013
NM_207361.6(FREM2):c.4150C>T (p.His1384Tyr) rs192340937 0.00012
NM_207361.6(FREM2):c.1369C>G (p.Leu457Val) rs141900626 0.00006
NM_207361.6(FREM2):c.1647C>A (p.Phe549Leu) rs114341997 0.00006
NM_207361.6(FREM2):c.2596T>A (p.Phe866Ile) rs566743573 0.00005
NM_207361.6(FREM2):c.1921A>G (p.Thr641Ala) rs116802472 0.00004
NM_207361.6(FREM2):c.2053G>A (p.Gly685Arg) rs773636566 0.00001
NM_207361.6(FREM2):c.332A>T (p.Asp111Val) rs761430669 0.00001
NM_207361.6(FREM2):c.3830T>G (p.Phe1277Cys) rs1437152125 0.00001
NM_207361.6(FREM2):c.5500A>G (p.Arg1834Gly) rs1162992431 0.00001
NM_207361.6(FREM2):c.5689G>T (p.Val1897Phe) rs1213042816 0.00001
NM_207361.6(FREM2):c.8777A>G (p.Tyr2926Cys) rs1878414292 0.00001
NM_207361.6(FREM2):c.1349A>G (p.Tyr450Cys)
NM_207361.6(FREM2):c.1364G>A (p.Arg455Gln) rs1217298919
NM_207361.6(FREM2):c.1823G>A (p.Gly608Glu) rs774621627
NM_207361.6(FREM2):c.2099C>A (p.Pro700His)
NM_207361.6(FREM2):c.2620C>T (p.His874Tyr)
NM_207361.6(FREM2):c.3035_3040dup (p.Gly1012_Ser1013dup) rs570476408
NM_207361.6(FREM2):c.304G>C (p.Gly102Arg) rs1869535237
NM_207361.6(FREM2):c.386G>T (p.Cys129Phe) rs745938776
NM_207361.6(FREM2):c.38G>T (p.Arg13Leu)
NM_207361.6(FREM2):c.4430T>C (p.Val1477Ala) rs1319182599
NM_207361.6(FREM2):c.4474A>G (p.Ile1492Val) rs2138071590
NM_207361.6(FREM2):c.4568G>A (p.Arg1523His)
NM_207361.6(FREM2):c.4901C>A (p.Thr1634Lys) rs74781600
NM_207361.6(FREM2):c.5059_5060inv (p.Glu1687Ser)
NM_207361.6(FREM2):c.5148C>A (p.Asn1716Lys) rs2138073287
NM_207361.6(FREM2):c.5293C>T (p.Arg1765Cys)
NM_207361.6(FREM2):c.5377C>T (p.Arg1793Cys)
NM_207361.6(FREM2):c.5434G>A (p.Ala1812Thr) rs749830746
NM_207361.6(FREM2):c.7136C>G (p.Ser2379Cys)
NM_207361.6(FREM2):c.8201G>A (p.Arg2734His)
NM_207361.6(FREM2):c.8381A>C (p.Gln2794Pro) rs2137937738
NM_207361.6(FREM2):c.8479C>T (p.Arg2827Cys)
NM_207361.6(FREM2):c.850G>C (p.Val284Leu) rs770004356
NM_207361.6(FREM2):c.8587A>G (p.Met2863Val)
NM_207361.6(FREM2):c.87GCT[8] (p.Leu38_Ser39insLeu)
NM_207361.6(FREM2):c.881G>A (p.Gly294Asp) rs1869591293

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