ClinVar Miner

List of variants in gene DMD reported as likely benign for Dilated cardiomyopathy 3B

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_004006.3(DMD):c.8734A>G (p.Asn2912Asp) rs1800278 0.02976
NM_004006.3(DMD):c.8729A>T (p.Glu2910Val) rs41305353 0.02876
NM_004006.3(DMD):c.5016T>A (p.Asn1672Lys) rs16990264 0.02084
NM_004006.3(DMD):c.2391T>G (p.Asn797Lys) rs72468681 0.00714
NM_004006.3(DMD):c.*2039C>A rs72466523 0.00578
NM_004006.3(DMD):c.10789C>T (p.Leu3597=) rs1800281 0.00486
NM_004006.3(DMD):c.7542+13A>G rs72466585 0.00407
NM_004006.3(DMD):c.3406A>T (p.Thr1136Ser) rs3827462 0.00356
NM_004006.3(DMD):c.*477T>C rs764294071 0.00278
NM_004006.3(DMD):c.*571A>G rs192963364 0.00275
NM_004006.3(DMD):c.*855G>A rs150236690 0.00211
NM_004006.3(DMD):c.8571T>C (p.Thr2857=) rs72466570 0.00153
NM_004006.3(DMD):c.*1705A>G rs145632098 0.00140
NM_004006.3(DMD):c.1888A>G (p.Thr630Ala) rs72468692 0.00124
NM_004006.3(DMD):c.5620G>A (p.Glu1874Lys) rs142441725 0.00119
NM_004006.3(DMD):c.5586+9G>A rs200025478 0.00044
NM_004006.3(DMD):c.*1035A>G rs112754560 0.00035
NM_004006.3(DMD):c.*1455C>A rs191747923 0.00023
NM_004006.3(DMD):c.5163G>C (p.Lys1721Asn) rs72468630 0.00021
NM_004006.3(DMD):c.1666G>A (p.Asp556Asn) rs182708940 0.00020
NM_004006.3(DMD):c.1809G>A (p.Leu603=) rs192176661 0.00020
NM_004006.3(DMD):c.9486G>A (p.Glu3162=) rs370724251 0.00015
NM_004006.3(DMD):c.7151C>A (p.Ser2384Tyr) rs185706283 0.00014
NM_004006.3(DMD):c.1184G>A (p.Arg395Gln) rs148511512 0.00006
NM_004006.3(DMD):c.*2563G>A rs188558013 0.00001
NM_004006.3(DMD):c.*1554TAAG[4] rs758612124
NM_004006.3(DMD):c.*2037_*2038dup rs200703281
NM_004006.3(DMD):c.-114dup rs72470542
NM_004006.3(DMD):c.-22G>A rs780710916
NM_004006.3(DMD):c.2273A>C (p.Asp758Ala) rs750526692
NM_004006.3(DMD):c.6291-10T>C rs758023750
NM_004006.3(DMD):c.94-9dup rs3834997

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