ClinVar Miner

List of variants in gene DMD reported as likely benign for Cardiovascular phenotype

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Gene type:
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Total variants: 35
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HGVS dbSNP
NM_004006.2(DMD):c.10836C>T (p.Ser3612=) rs148590546
NM_004006.2(DMD):c.1513G>C (p.Val505Leu) rs140340626
NM_004006.2(DMD):c.1575A>G (p.Ala525=) rs144372300
NM_004006.2(DMD):c.1812C>T (p.Ala604=) rs140919039
NM_004006.2(DMD):c.2331G>C (p.Leu777=) rs369659071
NM_004006.2(DMD):c.2331G>T (p.Leu777=) rs369659071
NM_004006.2(DMD):c.2745A>C (p.Thr915=) rs149922633
NM_004006.2(DMD):c.2973G>A (p.Glu991=) rs780454571
NM_004006.2(DMD):c.3360G>A (p.Glu1120=) rs754467083
NM_004006.2(DMD):c.3825G>A (p.Leu1275=) rs1379237787
NM_004006.2(DMD):c.3951G>A (p.Glu1317=) rs199643655
NM_004006.2(DMD):c.4125T>C (p.Thr1375=) rs144329742
NM_004006.2(DMD):c.4233+2C>T rs147474070
NM_004006.2(DMD):c.468A>C (p.Val156=) rs886044031
NM_004006.2(DMD):c.5265C>T (p.Pro1755=) rs145515413
NM_004006.2(DMD):c.5349G>A (p.Leu1783=) rs886039049
NM_004006.2(DMD):c.5620G>A (p.Glu1874Lys) rs142441725
NM_004006.2(DMD):c.6143G>A (p.Ser2048Asn) rs200494003
NM_004006.2(DMD):c.6471T>A (p.Thr2157=) rs377080659
NM_004006.2(DMD):c.7183G>A (p.Ala2395Thr) rs72466590
NM_004006.2(DMD):c.7243C>T (p.Arg2415Cys) rs139395045
NM_004006.2(DMD):c.7281A>G (p.Leu2427=) rs886038872
NM_004006.2(DMD):c.7359A>G (p.Glu2453=) rs780283825
NM_004006.2(DMD):c.7472A>G (p.Gln2491Arg) rs147694734
NM_004006.2(DMD):c.7521C>T (p.Asn2507=) rs112516305
NM_004006.2(DMD):c.802T>C (p.Leu268=) rs1800264
NM_004006.2(DMD):c.8076A>G (p.Gln2692=) rs144518527
NM_004006.2(DMD):c.8226A>G (p.Gln2742=) rs746514008
NM_004006.2(DMD):c.8571T>C (p.Thr2857=) rs72466570
NM_004006.2(DMD):c.8767G>T (p.Ala2923Ser) rs116283249
NM_004006.2(DMD):c.8976G>A (p.Val2992=) rs916865376
NM_004006.2(DMD):c.9165G>A (p.Thr3055=) rs137905486
NM_004006.2(DMD):c.9291C>T (p.Asp3097=) rs796934165
NM_004006.2(DMD):c.9486G>A (p.Glu3162=) rs370724251
NM_004006.2(DMD):c.9804A>G (p.Gln3268=) rs12690372

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