ClinVar Miner

List of variants in gene FREM1 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_144966.7(FREM1):c.-766A>C rs139022146 0.00838
NM_144966.6(FREM1):c.*2313T>C rs142822341 0.00683
NM_144966.6(FREM1):c.*2324T>A rs187661556 0.00457
NM_144966.6(FREM1):c.*334A>T rs75042646 0.00368
NM_144966.6(FREM1):c.*616G>A rs73411795 0.00318
NM_144966.6(FREM1):c.*2461C>A rs112050651 0.00310
NM_001379081.2(FREM1):c.6528C>T (p.Ser2176=) rs144454947 0.00247
NM_001379081.2(FREM1):c.4711G>A (p.Asp1571Asn) rs115421185 0.00244
NM_001379081.2(FREM1):c.*202G>C rs376485630 0.00189
NM_001379081.2(FREM1):c.1464C>T (p.Ser488=) rs200064797 0.00155
NM_001379081.2(FREM1):c.5205-14C>T rs77061232 0.00153
NM_001379081.2(FREM1):c.4442+3G>A rs181859461 0.00119
NM_001379081.2(FREM1):c.6279A>G (p.Val2093=) rs373107801 0.00033
NM_001379081.2(FREM1):c.4941C>T (p.Tyr1647=) rs373880888 0.00020
NM_001379081.2(FREM1):c.3404T>C (p.Ile1135Thr) rs187388944 0.00016
NM_144966.6(FREM1):c.*1844G>A rs10961688 0.00016
NM_001379081.2(FREM1):c.1329C>T (p.Asp443=) rs201393312 0.00009
NM_001379081.2(FREM1):c.571G>A (p.Gly191Arg) rs370556388 0.00009
NM_144966.6(FREM1):c.*2664A>G rs534652522 0.00009
NM_001379081.2(FREM1):c.-396C>T rs143700147 0.00006
NM_001379081.2(FREM1):c.1492C>T (p.Arg498Trp) rs200642807 0.00006
NM_001379081.2(FREM1):c.4879G>T (p.Ala1627Ser) rs370198850 0.00006
NM_144966.6(FREM1):c.*2405T>G rs183890666 0.00005
NM_001379081.2(FREM1):c.3932T>C (p.Ile1311Thr) rs182527895 0.00004
NM_001379081.2(FREM1):c.2212C>G (p.Gln738Glu) rs182946445
NM_001379081.2(FREM1):c.3517G>T (p.Ala1173Ser) rs564039071
NM_001379081.2(FREM1):c.5335-11dup rs140882884
NM_001379081.2(FREM1):c.5335-8dup rs201316684
NM_144966.6(FREM1):c.*1382dup rs35992592
NM_144966.6(FREM1):c.*530T>C rs570855729

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