ClinVar Miner

List of variants in gene MEGF8 reported as likely benign for acrocephalosyndactyly

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NM_001271938.2(MEGF8):c.1789-5C>T rs752609842
NM_001271938.2(MEGF8):c.1933+10C>T rs763206386
NM_001271938.2(MEGF8):c.2454C>T (p.Ser818=) rs140035679
NM_001271938.2(MEGF8):c.246G>T (p.Thr82=) rs369259465
NM_001271938.2(MEGF8):c.2537C>T (p.Ser846Leu) rs148207079
NM_001271938.2(MEGF8):c.2649T>C (p.Asp883=) rs757551016
NM_001271938.2(MEGF8):c.3033C>T (p.Thr1011=) rs145216125
NM_001271938.2(MEGF8):c.3310C>T (p.Arg1104Trp) rs370522595
NM_001271938.2(MEGF8):c.3378G>A (p.Val1126=) rs780556649
NM_001271938.2(MEGF8):c.351+10G>A rs374212597
NM_001271938.2(MEGF8):c.352-5C>T rs180788941
NM_001271938.2(MEGF8):c.3625C>T (p.Arg1209Trp) rs372257661
NM_001271938.2(MEGF8):c.3798C>T (p.Arg1266=) rs750232469
NM_001271938.2(MEGF8):c.3843G>A (p.Arg1281=) rs148792547
NM_001271938.2(MEGF8):c.3873G>A (p.Gly1291=) rs373710119
NM_001271938.2(MEGF8):c.390G>A (p.Leu130=) rs377093238
NM_001271938.2(MEGF8):c.4434C>T (p.Pro1478=) rs371090576
NM_001271938.2(MEGF8):c.5007C>A (p.Pro1669=) rs755932452
NM_001271938.2(MEGF8):c.6274-9C>G rs373417416
NM_001271938.2(MEGF8):c.6395G>A (p.Arg2132Gln) rs201140958
NM_001271938.2(MEGF8):c.6966C>T (p.Ser2322=) rs754666704
NM_001271938.2(MEGF8):c.7089C>T (p.Cys2363=) rs138235390
NM_001271938.2(MEGF8):c.7421G>A (p.Arg2474His) rs45623135
NM_001271938.2(MEGF8):c.7673C>T (p.Pro2558Leu) rs147216997
NM_001271938.2(MEGF8):c.7705G>A (p.Val2569Ile) rs147133204
NM_001271938.2(MEGF8):c.7893C>G (p.Ala2631=) rs150486662
NM_001271938.2(MEGF8):c.8133G>A (p.Pro2711=) rs370578585
NM_001271938.2(MEGF8):c.8176C>T (p.Arg2726Cys) rs141224456
NM_001271938.2(MEGF8):c.8271C>T (p.Pro2757=) rs755400663

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