ClinVar Miner

List of variants in gene TRPM4 reported as uncertain significance for cardiomyopathy

Included ClinVar conditions (519):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_017636.4(TRPM4):c.1139C>T (p.Ala380Val) rs150894548 0.00011
NM_017636.4(TRPM4):c.2732C>T (p.Thr911Met) rs148006852 0.00006
NM_017636.4(TRPM4):c.1603G>A (p.Glu535Lys) rs748187859 0.00004
NM_017636.4(TRPM4):c.3512G>A (p.Arg1171His) rs762615860 0.00003
NM_017636.4(TRPM4):c.1787T>C (p.Leu596Pro) rs946021556 0.00002
NM_017636.4(TRPM4):c.739A>T (p.Asn247Tyr) rs1555752067 0.00001
NM_017636.4(TRPM4):c.1039C>G (p.Leu347Val) rs1471303873
NM_017636.4(TRPM4):c.1496G>A (p.Arg499Gln) rs2122936347
NM_017636.4(TRPM4):c.337C>T (p.Arg113Cys)

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