ClinVar Miner

List of variants in gene MYH9 reported as uncertain significance for Fechtner syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_002473.5(MYH9):c.1730T>C (p.Val577Ala)
NM_002473.5(MYH9):c.193G>A (p.Val65Met) rs377348805
NM_002473.5(MYH9):c.2714G>A (p.Arg905His) rs727503289
NM_002473.5(MYH9):c.4261G>A (p.Glu1421Lys) rs1569534914
NM_002473.5(MYH9):c.5081G>A (p.Arg1694His) rs538330756
NM_002473.5(MYH9):c.5275-7_5275-5del rs780656298
NM_002473.5(MYH9):c.5456T>G (p.Leu1819Arg) rs368440234
NM_002473.5(MYH9):c.658G>A (p.Ala220Thr) rs1556637683

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