List of variants reported as uncertain significance for dilated cardiomyopathy 3B by Fulgent Genetics, Fulgent Genetics

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 104

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.-188C>T	rs886043394	0.00018
NM_004006.3(DMD):c.357+5G>A	rs778431187	0.00013
NM_004006.3(DMD):c.295A>G (p.Ile99Val)	rs149428656	0.00011
NM_004006.3(DMD):c.-75G>A	rs778938887	0.00009
NM_004006.3(DMD):c.6409G>C (p.Glu2137Gln)	rs1023328955	0.00009
NM_004006.3(DMD):c.8053G>A (p.Glu2685Lys)	rs748937055	0.00007
NM_004006.3(DMD):c.9580A>C (p.Ile3194Leu)	rs181517869	0.00007
NM_004006.3(DMD):c.6863A>G (p.Gln2288Arg)	rs762708936	0.00006
NM_004006.3(DMD):c.8399T>C (p.Leu2800Ser)	rs398124071	0.00006
NM_004006.3(DMD):c.146G>A (p.Arg49His)	rs765584669	0.00005
NM_004006.3(DMD):c.1654G>T (p.Val552Phe)	rs748690103	0.00005
NM_004006.3(DMD):c.1687C>T (p.Arg563Cys)	rs145739725	0.00005
NM_004006.3(DMD):c.5270T>C (p.Ile1757Thr)	rs201516290	0.00005
NM_004006.3(DMD):c.7712G>T (p.Arg2571Leu)	rs371588290	0.00005
NM_004006.3(DMD):c.8321T>G (p.Leu2774Arg)	rs750419527	0.00005
NM_004006.3(DMD):c.8609G>A (p.Arg2870Gln)	rs373481995	0.00005
NM_004006.3(DMD):c.9504G>C (p.Leu3168Phe)	rs185247491	0.00005
NM_004006.3(DMD):c.1534C>T (p.His512Tyr)	rs147136371	0.00004
NM_004006.3(DMD):c.2346A>T (p.Arg782Ser)	rs150692967	0.00004
NM_004006.3(DMD):c.4000G>A (p.Gly1334Arg)	rs146880270	0.00004
NM_004006.3(DMD):c.1183C>T (p.Arg395Trp)	rs780356433	0.00003
NM_004006.3(DMD):c.1988C>T (p.Ala663Val)	rs41309715	0.00003
NM_004006.3(DMD):c.2323A>G (p.Arg775Gly)	rs886038905	0.00003
NM_004006.3(DMD):c.2518C>G (p.Gln840Glu)	rs398123892	0.00003
NM_004006.3(DMD):c.2912A>T (p.Asp971Val)	rs762154042	0.00003
NM_004006.3(DMD):c.3344T>C (p.Ile1115Thr)	rs748123444	0.00003
NM_004006.3(DMD):c.4483C>G (p.Gln1495Glu)	rs748769566	0.00003
NM_004006.3(DMD):c.5869C>T (p.Arg1957Trp)	rs755477994	0.00003
NM_004006.3(DMD):c.626T>C (p.Ile209Thr)	rs372832497	0.00003
NM_004006.3(DMD):c.6572G>A (p.Arg2191Gln)	rs756238158	0.00003
NM_004006.3(DMD):c.8239G>A (p.Ala2747Thr)	rs772732788	0.00003
NM_004006.3(DMD):c.10615C>G (p.Leu3539Val)	rs367748290	0.00002
NM_004006.3(DMD):c.1094A>G (p.Gln365Arg)	rs1216968523	0.00002
NM_004006.3(DMD):c.11015-5T>A	rs753104670	0.00002
NM_004006.3(DMD):c.11023A>G (p.Thr3675Ala)	rs768016083	0.00002
NM_004006.3(DMD):c.1463G>A (p.Arg488His)	rs794727065	0.00002
NM_004006.3(DMD):c.1536C>A (p.His512Gln)	rs776446238	0.00002
NM_004006.3(DMD):c.2233C>G (p.Pro745Ala)	rs1435295333	0.00002
NM_004006.3(DMD):c.2726C>T (p.Ala909Val)	rs370014420	0.00002
NM_004006.3(DMD):c.298G>A (p.Val100Ile)	rs779099343	0.00002
NM_004006.3(DMD):c.3029C>T (p.Ala1010Val)	rs780896933	0.00002
NM_004006.3(DMD):c.3232C>T (p.Leu1078Phe)	rs375329908	0.00002
NM_004006.3(DMD):c.3619G>A (p.Ala1207Thr)	rs1448639542	0.00002
NM_004006.3(DMD):c.3953A>G (p.Asp1318Gly)	rs759820971	0.00002
NM_004006.3(DMD):c.4728G>C (p.Met1576Ile)	rs757160024	0.00002
NM_004006.3(DMD):c.5022G>T (p.Leu1674Phe)	rs398123975	0.00002
NM_004006.3(DMD):c.5863C>T (p.Arg1955Cys)	rs377039314	0.00002
NM_004006.3(DMD):c.6787C>T (p.Arg2263Cys)	rs200045725	0.00002
NM_004006.3(DMD):c.7429C>T (p.Arg2477Trp)	rs759274835	0.00002
NM_004006.3(DMD):c.7585G>C (p.Glu2529Gln)	rs771509836	0.00002
NM_004006.3(DMD):c.7711C>T (p.Arg2571Trp)	rs757011771	0.00002
NM_004006.3(DMD):c.772C>A (p.Pro258Thr)	rs773066825	0.00002
NM_004006.3(DMD):c.10213A>G (p.Asn3405Asp)	rs770516401	0.00001
NM_004006.3(DMD):c.10712G>A (p.Arg3571His)	rs935091512	0.00001
NM_004006.3(DMD):c.10915T>C (p.Ser3639Pro)	rs990606875	0.00001
NM_004006.3(DMD):c.1109A>T (p.Asn370Ile)	rs773299186	0.00001
NM_004006.3(DMD):c.1388G>T (p.Trp463Leu)	rs863224981	0.00001
NM_004006.3(DMD):c.1648C>T (p.Arg550Cys)	rs778354538	0.00001
NM_004006.3(DMD):c.1749C>G (p.Asn583Lys)	rs775846754	0.00001
NM_004006.3(DMD):c.2017C>G (p.Gln673Glu)	rs128626232	0.00001
NM_004006.3(DMD):c.2039C>A (p.Thr680Asn)	rs367769606	0.00001
NM_004006.3(DMD):c.2079G>T (p.Gln693His)	rs761441684	0.00001
NM_004006.3(DMD):c.2312C>T (p.Ala771Val)	rs1245604423	0.00001
NM_004006.3(DMD):c.2551A>C (p.Asn851His)	rs753665097	0.00001
NM_004006.3(DMD):c.2764T>G (p.Phe922Val)	rs185395584	0.00001
NM_004006.3(DMD):c.3982C>G (p.Gln1328Glu)	rs745640786	0.00001
NM_004006.3(DMD):c.4404G>T (p.Glu1468Asp)	rs1462655612	0.00001
NM_004006.3(DMD):c.5146G>A (p.Val1716Met)	rs748814615	0.00001
NM_004006.3(DMD):c.5156G>A (p.Arg1719His)	rs1273883368	0.00001
NM_004006.3(DMD):c.5506C>G (p.Gln1836Glu)	rs770845480	0.00001
NM_004006.3(DMD):c.5741A>G (p.Glu1914Gly)	rs985546923	0.00001
NM_004006.3(DMD):c.6455T>C (p.Ile2152Thr)	rs767681834	0.00001
NM_004006.3(DMD):c.7490G>T (p.Arg2497Met)	rs1312256471	0.00001
NM_004006.3(DMD):c.74T>C (p.Val25Ala)	rs886039061	0.00001
NM_004006.3(DMD):c.7799G>T (p.Arg2600Ile)	rs747127624	0.00001
NM_004006.3(DMD):c.8072T>C (p.Leu2691Pro)	rs748485762	0.00001
NM_004006.3(DMD):c.836C>T (p.Thr279Met)	rs369135184	0.00001
NM_004006.3(DMD):c.8704C>T (p.Arg2902Trp)	rs1188233243	0.00001
NM_004006.3(DMD):c.1097G>A (p.Gly366Glu)	rs763144501
NM_004006.3(DMD):c.1693A>T (p.Thr565Ser)	rs766450050
NM_004006.3(DMD):c.1788G>A (p.Met596Ile)	rs2052669244
NM_004006.3(DMD):c.1826A>G (p.Asp609Gly)	rs2149095572
NM_004006.3(DMD):c.1851G>A (p.Met617Ile)	rs1238073206
NM_004006.3(DMD):c.1915A>C (p.Lys639Gln)	rs2149094935
NM_004006.3(DMD):c.2273A>G (p.Asp758Gly)	rs750526692
NM_004006.3(DMD):c.2330T>C (p.Leu777Pro)	rs794727226
NM_004006.3(DMD):c.3137A>C (p.Gln1046Pro)	rs2040288189
NM_004006.3(DMD):c.3190A>G (p.Met1064Val)	rs1281398911
NM_004006.3(DMD):c.365A>C (p.Asn122Thr)	rs1603437369
NM_004006.3(DMD):c.3954T>A (p.Asp1318Glu)	rs2098269308
NM_004006.3(DMD):c.4477G>A (p.Val1493Met)	rs2097986154
NM_004006.3(DMD):c.4741A>G (p.Asn1581Asp)	rs727503831
NM_004006.3(DMD):c.4899G>T (p.Glu1633Asp)	rs886044407
NM_004006.3(DMD):c.4987G>A (p.Val1663Ile)	rs2147259228
NM_004006.3(DMD):c.5324_5325delinsGT (p.Lys1775Ser)	rs1557303381
NM_004006.3(DMD):c.5922+3G>C	rs398124000
NM_004006.3(DMD):c.6471TGT[3] (p.Val2159dup)	rs1395996899
NM_004006.3(DMD):c.6839G>A (p.Ser2280Asn)	rs1060502614
NM_004006.3(DMD):c.7514A>T (p.Asp2505Val)	rs2090505173
NM_004006.3(DMD):c.803T>C (p.Leu268Ser)	rs939491009
NM_004006.3(DMD):c.8150A>G (p.Asp2717Gly)	rs886043271
NM_004006.3(DMD):c.8794A>T (p.Thr2932Ser)	rs2067958322
NM_004006.3(DMD):c.9352G>T (p.Ala3118Ser)	rs200928985
NM_004006.3(DMD):c.960G>A (p.Gln320=)	rs772656026

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