ClinVar Miner

List of variants in gene combination C2orf49, FHL2 reported as likely benign for Primary dilated cardiomyopathy

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_001318895.3(FHL2):c.337C>T (p.Arg113Cys) rs140148322 0.00032
NM_001318895.3(FHL2):c.738C>T (p.Asn246=) rs755230829 0.00023
NM_001318895.3(FHL2):c.174C>T (p.Asp58=) rs141208906 0.00020
NM_001318895.3(FHL2):c.507C>T (p.Ile169=) rs539301452 0.00013
NM_001318895.3(FHL2):c.486C>T (p.Cys162=) rs373978741 0.00004
NM_001318895.3(FHL2):c.261G>C (p.Leu87=) rs758881698 0.00003
NM_001318895.3(FHL2):c.462T>C (p.Tyr154=) rs397517960 0.00003
NM_001318895.3(FHL2):c.501+8A>T rs1033789814 0.00002
NM_001318895.3(FHL2):c.502-16C>T rs1278363053 0.00002
NM_001318895.3(FHL2):c.651T>C (p.Tyr217=) rs1045935903 0.00002
NM_001318895.3(FHL2):c.688+7G>A rs768230517 0.00002
NM_001318895.3(FHL2):c.157-14G>A rs1681265871 0.00001
NM_001318895.3(FHL2):c.157-9G>A rs750799536 0.00001
NM_001318895.3(FHL2):c.291C>T (p.Tyr97=) rs767220225 0.00001
NM_001318895.3(FHL2):c.333T>C (p.Gly111=) rs780800767 0.00001
NM_001318895.3(FHL2):c.502-10G>A rs779913648 0.00001
NM_001318895.3(FHL2):c.502-11C>T rs750695509 0.00001
NM_001318895.3(FHL2):c.513G>A (p.Thr171=) rs1018740778 0.00001
NM_001318895.3(FHL2):c.540C>T (p.Pro180=) rs1210749693 0.00001
NM_001318895.3(FHL2):c.609C>T (p.Arg203=) rs745753003 0.00001
NM_001318895.3(FHL2):c.688+11C>T rs1218219091 0.00001
NM_001318895.3(FHL2):c.720G>A (p.Glu240=) rs777732229 0.00001
NM_001318895.3(FHL2):c.157-8C>T
NM_001318895.3(FHL2):c.186T>C (p.His62=) rs1462640060
NM_001318895.3(FHL2):c.243T>C (p.Ala81=) rs1573306617
NM_001318895.3(FHL2):c.252G>A (p.Glu84=)
NM_001318895.3(FHL2):c.270A>G (p.Thr90=) rs753388370
NM_001318895.3(FHL2):c.285C>T (p.Asn95=) rs374383740
NM_001318895.3(FHL2):c.331+10C>A rs776981929
NM_001318895.3(FHL2):c.332-11C>T
NM_001318895.3(FHL2):c.332-11_332-3del rs1257906826
NM_001318895.3(FHL2):c.332-14G>T rs1680740003
NM_001318895.3(FHL2):c.332-6T>C
NM_001318895.3(FHL2):c.336C>T (p.Thr112=) rs140501334
NM_001318895.3(FHL2):c.351C>T (p.Tyr117=) rs1553415161
NM_001318895.3(FHL2):c.354G>A (p.Lys118=)
NM_001318895.3(FHL2):c.414C>A (p.Thr138=) rs1013627686
NM_001318895.3(FHL2):c.414C>T (p.Thr138=) rs1013627686
NM_001318895.3(FHL2):c.429C>T (p.Pro143=) rs2467175797
NM_001318895.3(FHL2):c.501+16C>T rs767774355
NM_001318895.3(FHL2):c.501+17C>T rs761990478
NM_001318895.3(FHL2):c.501+20G>C
NM_001318895.3(FHL2):c.502-12T>C rs2467152387
NM_001318895.3(FHL2):c.502-13C>G rs754663221
NM_001318895.3(FHL2):c.502-13C>T
NM_001318895.3(FHL2):c.502-5T>C rs2104487279
NM_001318895.3(FHL2):c.513G>C (p.Thr171=) rs1018740778
NM_001318895.3(FHL2):c.525T>C (p.Thr175=)
NM_001318895.3(FHL2):c.558C>T (p.Phe186=)
NM_001318895.3(FHL2):c.567C>T (p.Thr189=)
NM_001318895.3(FHL2):c.576G>A (p.Arg192=) rs747844229
NM_001318895.3(FHL2):c.594G>A (p.Gln198=)
NM_001318895.3(FHL2):c.612T>C (p.Asp204=) rs777181609
NM_001318895.3(FHL2):c.675C>A (p.Thr225=) rs1426474074
NM_001318895.3(FHL2):c.711C>A (p.Ile237=)
NM_001318895.3(FHL2):c.735T>C (p.His245=) rs1573267301
NM_001318895.3(FHL2):c.759G>A (p.Lys253=) rs1680246034
NM_001318895.3(FHL2):c.801G>A (p.Arg267=) rs1573266848
NM_001318895.3(FHL2):c.816C>T (p.Cys272=) rs1573266714

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