ClinVar Miner

List of variants in gene combination FLNA, LOC107988032 reported as likely benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_001110556.2(FLNA):c.7564G>A (p.Val2522Ile) rs187774579
NM_001110556.2(FLNA):c.7569C>T (p.Ser2523=)
NM_001110556.2(FLNA):c.7649C>T (p.Pro2550Leu) rs371724771
NM_001110556.2(FLNA):c.7668C>T (p.Asp2556=)
NM_001110556.2(FLNA):c.7725G>A (p.Lys2575=) rs782375435
NM_001110556.2(FLNA):c.7776G>C (p.Val2592=) rs369380495
NM_001110556.2(FLNA):c.7824C>T (p.His2608=) rs782530835
NM_001110556.2(FLNA):c.7835G>A (p.Arg2612Gln) rs200883457
NM_001110556.2(FLNA):c.7878C>T (p.Tyr2626=) rs782774918
NM_001110556.2(FLNA):c.7903G>A (p.Glu2635Lys) rs369717556

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