ClinVar Miner

List of variants reported as likely benign for Brugada syndrome by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (45):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_001378969.1(KCND3):c.669G>C (p.Ser223=) rs17215423 0.01872
NM_001037.5(SCN1B):c.591-14C>A rs28365109 0.00920
NM_201596.3(CACNB2):c.1785C>T (p.His595=) rs61733967 0.00879
NM_015141.4(GPD1L):c.81T>C (p.Asn27=) rs34278284 0.00515
NM_000335.5(SCN5A):c.1381T>G (p.Leu461Val) rs41313697 0.00352
NM_000719.7(CACNA1C):c.109G>A (p.Gly37Arg) rs34534613 0.00346
NM_201596.3(CACNB2):c.915T>C (p.Phe305=) rs149586418 0.00282
NM_001037.5(SCN1B):c.267C>T (p.Arg89=) rs140949982 0.00232
NM_001040151.2(SCN3B):c.582C>T (p.Asn194=) rs34964168 0.00232
NM_001037.5(SCN1B):c.448+321G>A rs72558028 0.00173
NM_001378969.1(KCND3):c.117T>C (p.Asp39=) rs12720446 0.00128
NM_000719.7(CACNA1C):c.1074G>A (p.Gln358=) rs139842134 0.00113
NM_000335.5(SCN5A):c.3266C>T (p.Pro1089Leu) rs1805125 0.00071
NM_015141.4(GPD1L):c.619-9C>G rs2044880 0.00057
NM_000335.5(SCN5A):c.1335C>T (p.His445=) rs368045716 0.00048
NM_001378969.1(KCND3):c.1131G>T (p.Thr377=) rs148428571 0.00038
NM_005477.3(HCN4):c.561T>C (p.Ala187=) rs375206856 0.00030
NM_000719.7(CACNA1C):c.5885G>A (p.Arg1962Gln) rs199776761 0.00026
NM_015141.4(GPD1L):c.459C>T (p.Asn153=) rs375532052 0.00019
NM_000719.7(CACNA1C):c.4957-15C>T rs766975739 0.00016
NM_005477.3(HCN4):c.2904G>A (p.Pro968=) rs368145651 0.00016
NM_015141.4(GPD1L):c.1038C>T (p.Ser346=) rs147092668 0.00016
NM_201596.3(CACNB2):c.102G>T (p.Ala34=) rs370839320 0.00013
NM_015141.4(GPD1L):c.959+11C>T rs370985609 0.00011
NM_000719.7(CACNA1C):c.5022C>T (p.Thr1674=) rs372300407 0.00010
NM_000719.7(CACNA1C):c.5444+719G>A rs765829807 0.00009
NM_201596.3(CACNB2):c.334-7A>T rs779728445 0.00009
NM_005477.3(HCN4):c.3351G>A (p.Pro1117=) rs375138488 0.00007
NM_000719.7(CACNA1C):c.6339C>T (p.Asp2113=) rs374843203 0.00006
NM_015141.4(GPD1L):c.367-10A>T rs113764055 0.00006
NM_000719.7(CACNA1C):c.2339+18C>T rs778390407 0.00005
NM_000719.7(CACNA1C):c.102G>A (p.Ala34=) rs376345869 0.00004
NM_000719.7(CACNA1C):c.2637G>A (p.Ala879=) rs199629800 0.00004
NM_000719.7(CACNA1C):c.3567C>T (p.Cys1189=) rs202058956 0.00004
NM_000719.7(CACNA1C):c.5277G>A (p.Ser1759=) rs371931644 0.00004
NM_015141.4(GPD1L):c.367-11C>A rs113202696 0.00004
NM_000335.5(SCN5A):c.1557T>C (p.Ser519=) rs371560571 0.00003
NM_000719.7(CACNA1C):c.285C>T (p.Thr95=) rs768096981 0.00003
NM_000719.7(CACNA1C):c.5493G>A (p.Thr1831=) rs368046891 0.00003
NM_000335.5(SCN5A):c.1677A>G (p.Thr559=) rs376389170 0.00002
NM_000335.5(SCN5A):c.1992C>T (p.Ser664=) rs368167264 0.00002
NM_000719.7(CACNA1C):c.6282C>G (p.Leu2094=) rs1337662531 0.00002
NM_005477.3(HCN4):c.1401C>T (p.Tyr467=) rs753580737 0.00002
NM_005477.3(HCN4):c.2916C>T (p.Pro972=) rs559422705 0.00002
NM_201596.3(CACNB2):c.1749C>G (p.Ala583=) rs755387775 0.00002
NM_000335.5(SCN5A):c.2694G>A (p.Glu898=) rs2061655979 0.00001
NM_000335.5(SCN5A):c.786C>T (p.Ser262=) rs753246399 0.00001
NM_000719.7(CACNA1C):c.3246C>T (p.Asp1082=) rs370662635 0.00001
NM_000719.7(CACNA1C):c.4857C>T (p.Tyr1619=) rs758486779 0.00001
NM_000719.7(CACNA1C):c.5157C>G (p.Pro1719=) rs534589273 0.00001
NM_000719.7(CACNA1C):c.6039C>T (p.Pro2013=) rs780157730 0.00001
NM_001037.5(SCN1B):c.396C>T (p.Tyr132=) rs181115510 0.00001
NM_005477.3(HCN4):c.3261C>T (p.Ser1087=) rs537717251 0.00001
NM_201596.3(CACNB2):c.1683G>A (p.Glu561=) rs773373763 0.00001
NM_201596.3(CACNB2):c.909G>A (p.Ala303=) rs144509796 0.00001
NM_000335.5(SCN5A):c.168G>A (p.Leu56=) rs376742447
NM_000335.5(SCN5A):c.795C>T (p.Ala265=) rs527692731
NM_001378969.1(KCND3):c.1041G>A (p.Ser347=) rs369361457
NM_001378969.1(KCND3):c.63G>C (p.Pro21=) rs923682288
NM_015141.4(GPD1L):c.367-11_367-10delinsAT rs1575115586
NM_201596.3(CACNB2):c.1055-7T>C rs201997903
NM_201596.3(CACNB2):c.1670C>T (p.Ser557Leu) rs137886839

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