ClinVar Miner

List of variants reported as likely benign for atrial fibrillation, familial, 18

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 85
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HGVS dbSNP gnomAD frequency
NM_002476.2(MYL4):c.167T>C (p.Phe56Ser) rs144870368 0.00147
NM_002476.2(MYL4):c.565+12C>T rs144326821 0.00066
NM_002476.2(MYL4):c.565+19C>T rs145181954 0.00014
NM_002476.2(MYL4):c.201G>A (p.Pro67=) rs149036573 0.00011
NM_002476.2(MYL4):c.339T>G (p.Phe113Leu) rs200195383 0.00011
NM_002476.2(MYL4):c.405C>T (p.Phe135=) rs150593274 0.00011
NM_002476.2(MYL4):c.565+13G>A rs374440892 0.00006
NM_002476.2(MYL4):c.565+17T>C rs576910138 0.00006
NM_002476.2(MYL4):c.313+9G>A rs1418767431 0.00004
NM_002476.2(MYL4):c.447G>A (p.Thr149=) rs371944933 0.00004
NM_002476.2(MYL4):c.471C>T (p.His157=) rs781162398 0.00004
NM_002476.2(MYL4):c.234C>T (p.Cys78=) rs138710476 0.00003
NM_002476.2(MYL4):c.313+16T>C rs376080778 0.00003
NM_002476.2(MYL4):c.225C>T (p.Tyr75=) rs372355856 0.00002
NM_002476.2(MYL4):c.345G>A (p.Thr115=) rs372522881 0.00002
NM_002476.2(MYL4):c.381G>A (p.Lys127=) rs557505985 0.00002
NM_002476.2(MYL4):c.72A>C (p.Ala24=) rs370547497 0.00002
NM_002476.2(MYL4):c.163+16C>T rs1598654437 0.00001
NM_002476.2(MYL4):c.163+17C>G rs368658322 0.00001
NM_002476.2(MYL4):c.164-13C>G rs770170911 0.00001
NM_002476.2(MYL4):c.276C>T (p.Ala92=) rs1343489917 0.00001
NM_002476.2(MYL4):c.314-16C>T rs770647651 0.00001
NM_002476.2(MYL4):c.315G>A (p.Glu105=) rs762424935 0.00001
NM_002476.2(MYL4):c.348C>T (p.Phe116=) rs184779796 0.00001
NM_002476.2(MYL4):c.351G>A (p.Leu117=) rs756774414 0.00001
NM_002476.2(MYL4):c.429C>T (p.Asp143=) rs139239258 0.00001
NM_002476.2(MYL4):c.487+14G>A rs1282938957 0.00001
NM_002476.2(MYL4):c.488-10C>A rs1438189931 0.00001
NM_002476.2(MYL4):c.522G>A (p.Leu174=) rs767533462 0.00001
NM_002476.2(MYL4):c.537G>A (p.Glu179=) rs181540609 0.00001
NM_002476.2(MYL4):c.549C>T (p.Gly183=) rs766393545 0.00001
NM_002476.2(MYL4):c.565+10C>T rs778856429 0.00001
NM_002476.2(MYL4):c.565+7A>G rs1443839567 0.00001
NM_002476.2(MYL4):c.567C>T (p.Ala189=) rs777538559 0.00001
NM_002476.2(MYL4):c.576G>A (p.Lys192=) rs1289546978 0.00001
NM_002476.2(MYL4):c.57A>G (p.Pro19=) rs765876288 0.00001
NM_002476.2(MYL4):c.66C>T (p.Ala22=) rs201301071 0.00001
NM_002476.2(MYL4):c.102C>T (p.Pro34=) rs968141146
NM_002476.2(MYL4):c.129T>C (p.Ser43=)
NM_002476.2(MYL4):c.135+10G>A
NM_002476.2(MYL4):c.135+14A>G rs760301323
NM_002476.2(MYL4):c.135+18A>T
NM_002476.2(MYL4):c.135+19T>C
NM_002476.2(MYL4):c.136-12C>T
NM_002476.2(MYL4):c.150C>G (p.Ala50=) rs143234546
NM_002476.2(MYL4):c.163+17C>A rs368658322
NM_002476.2(MYL4):c.164-16G>A rs1371912264
NM_002476.2(MYL4):c.164-20G>A rs934835262
NM_002476.2(MYL4):c.164-4A>C rs2149047338
NM_002476.2(MYL4):c.164-8C>T rs893225315
NM_002476.2(MYL4):c.171A>G (p.Lys57=)
NM_002476.2(MYL4):c.184T>C (p.Leu62=) rs1366120596
NM_002476.2(MYL4):c.207A>T (p.Gly69=) rs753325178
NM_002476.2(MYL4):c.252C>T (p.Ala84=) rs1598659253
NM_002476.2(MYL4):c.255G>A (p.Leu85=)
NM_002476.2(MYL4):c.291G>T (p.Val97=) rs2547598374
NM_002476.2(MYL4):c.300G>A (p.Lys100=) rs2064844083
NM_002476.2(MYL4):c.313+13G>T
NM_002476.2(MYL4):c.313+19C>T rs2064844435
NM_002476.2(MYL4):c.313+8C>A rs372826462
NM_002476.2(MYL4):c.313+8C>T rs372826462
NM_002476.2(MYL4):c.314-15C>T
NM_002476.2(MYL4):c.314-6C>T rs2149048609
NM_002476.2(MYL4):c.314-9T>C rs2547599570
NM_002476.2(MYL4):c.331C>T (p.Leu111=)
NM_002476.2(MYL4):c.396T>C (p.Tyr132=) rs746843611
NM_002476.2(MYL4):c.411G>A (p.Glu137=)
NM_002476.2(MYL4):c.435G>A (p.Glu145=)
NM_002476.2(MYL4):c.441T>C (p.Asn147=) rs1567749945
NM_002476.2(MYL4):c.474C>T (p.Val158=) rs2149048808
NM_002476.2(MYL4):c.487+13G>A rs1223343679
NM_002476.2(MYL4):c.487+20A>C rs2149048835
NM_002476.2(MYL4):c.488-12A>C
NM_002476.2(MYL4):c.488-15C>T
NM_002476.2(MYL4):c.488-9C>A rs1180756106
NM_002476.2(MYL4):c.504G>A (p.Glu168=) rs2547600399
NM_002476.2(MYL4):c.565+11G>T rs187128906
NM_002476.2(MYL4):c.565+12C>A rs144326821
NM_002476.2(MYL4):c.565+13G>C
NM_002476.2(MYL4):c.582C>A (p.Ile194=) rs1405716390
NM_002476.2(MYL4):c.588A>G (p.Ser196=) rs2547601071
NM_002476.2(MYL4):c.66C>G (p.Ala22=)
NM_002476.2(MYL4):c.6T>C (p.Ala2=) rs2547591092
NM_002476.2(MYL4):c.72A>G (p.Ala24=) rs370547497
NM_002476.2(MYL4):c.84C>G (p.Ala28=)

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