ClinVar Miner

List of variants in gene KCND3 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001378969.1(KCND3):c.*225T>C rs72548736 0.01430
NM_001378969.1(KCND3):c.-72-284C>A rs140731277 0.01402
NM_001378969.1(KCND3):c.1519-67A>G rs72548731 0.01243
NM_001378969.1(KCND3):c.1372-34G>A rs72548728 0.01200
NM_001378969.1(KCND3):c.1270-153G>C rs79167507 0.01192
NM_001378969.1(KCND3):c.-72-245C>T rs147254704 0.01106
NM_001378969.1(KCND3):c.1519-96G>A rs147765490 0.00798
NM_001378969.1(KCND3):c.1106+296G>T rs75584783 0.00631
NM_001378969.1(KCND3):c.-72-119T>C rs142774938 0.00446
NM_001378969.1(KCND3):c.627G>C (p.Thr209=) rs149299911 0.00182
NM_001378969.1(KCND3):c.117T>C (p.Asp39=) rs12720446 0.00128
NM_001378969.1(KCND3):c.1573A>G (p.Met525Val) rs145890206 0.00076
NM_001378969.1(KCND3):c.1131G>T (p.Thr377=) rs148428571 0.00038
NM_001378969.1(KCND3):c.641A>G (p.Lys214Arg) rs142744204 0.00034
NM_001378969.1(KCND3):c.1959C>T (p.Ser653=) rs147087785 0.00027
NM_001378969.1(KCND3):c.459G>A (p.Ser153=) rs755206508 0.00018
NM_001378969.1(KCND3):c.1106+10C>T rs377267051 0.00016
NM_001378969.1(KCND3):c.1354G>A (p.Glu452Lys) rs200532657 0.00012
NM_001378969.1(KCND3):c.-30G>A rs753351881 0.00010
NM_001378969.1(KCND3):c.-36G>C rs200106311 0.00010
NM_001378969.1(KCND3):c.1269+13C>T rs72548726 0.00009
NM_001378969.1(KCND3):c.1766+3G>A rs748524463 0.00009
NM_001378969.1(KCND3):c.1348C>T (p.Leu450Phe) rs150401343 0.00006
NM_001378969.1(KCND3):c.651G>A (p.Pro217=) rs186974111 0.00006
NM_001378969.1(KCND3):c.1308C>G (p.Gly436=) rs190703406 0.00005
NM_001378969.1(KCND3):c.-73+753A>G rs539046437 0.00003
NM_001378969.1(KCND3):c.1416C>T (p.Ile472=) rs374945628 0.00003
NM_001378969.1(KCND3):c.879C>T (p.Arg293=) rs147739517 0.00002
NM_001378969.1(KCND3):c.1359G>A (p.Ala453=) rs762936059 0.00001
NM_001378969.1(KCND3):c.186G>A (p.Pro62=) rs1411627342 0.00001
NM_001378969.1(KCND3):c.342C>T (p.Tyr114=) rs555413116 0.00001
NM_001378969.1(KCND3):c.528C>G (p.Pro176=) rs370342092 0.00001
NM_001378969.1(KCND3):c.727C>T (p.Leu243=) rs769885163 0.00001
NM_001378969.1(KCND3):c.786C>T (p.Ile262=) rs369172530 0.00001
NM_001378969.1(KCND3):c.*257dup rs72548738
NM_001378969.1(KCND3):c.-27del rs371333782
NM_001378969.1(KCND3):c.-47G>C rs776077160
NM_001378969.1(KCND3):c.1372-112dup rs72548727
NM_001378969.1(KCND3):c.1372-6dup rs769051410
NM_001378969.1(KCND3):c.1519-4G>A rs72548732
NM_001378969.1(KCND3):c.1766+224dup rs965649464
NM_001378969.1(KCND3):c.633G>T (p.Pro211=) rs35131566

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