ClinVar Miner

List of variants in gene MYL4 reported as likely benign for atrial fibrillation (disease)

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_002476.2(MYL4):c.164-8C>T
NM_002476.2(MYL4):c.167T>C (p.Phe56Ser) rs144870368
NM_002476.2(MYL4):c.201G>A (p.Pro67=) rs149036573
NM_002476.2(MYL4):c.252C>T (p.Ala84=) rs1598659253
NM_002476.2(MYL4):c.276C>T (p.Ala92=)
NM_002476.2(MYL4):c.313+8C>A rs372826462
NM_002476.2(MYL4):c.313+8C>T
NM_002476.2(MYL4):c.339T>G (p.Phe113Leu) rs200195383
NM_002476.2(MYL4):c.345G>A (p.Thr115=) rs372522881
NM_002476.2(MYL4):c.381G>A (p.Lys127=)
NM_002476.2(MYL4):c.405C>T (p.Phe135=) rs150593274
NM_002476.2(MYL4):c.447G>A (p.Thr149=) rs371944933
NM_002476.2(MYL4):c.471C>T (p.His157=)
NM_002476.2(MYL4):c.522G>A (p.Leu174=) rs767533462
NM_002476.2(MYL4):c.537G>A (p.Glu179=) rs181540609
NM_002476.2(MYL4):c.567C>T (p.Ala189=)
NM_002476.2(MYL4):c.582C>A (p.Ile194=) rs1405716390

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