ClinVar Miner

List of variants in gene combination CACNB2, NSUN6 reported as likely benign for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP
NM_201590.2(CACNB2):c.1044+4_1044+7dupAGTA rs1456201116
NM_201590.3(CACNB2):c.*10G>T rs4747352
NM_201590.3(CACNB2):c.*1330_*1333dup rs33980121
NM_201590.3(CACNB2):c.*1665T>C rs80130376
NM_201590.3(CACNB2):c.*17T>C rs58830289
NM_201590.3(CACNB2):c.*1965C>T rs10828872
NM_201590.3(CACNB2):c.*2016T>C rs7079776
NM_201590.3(CACNB2):c.*463_*466dup rs373389018
NM_201590.3(CACNB2):c.*516_*519dup rs201149401
NM_201590.3(CACNB2):c.*52_*55dup rs199830080
NM_201590.3(CACNB2):c.*571_*573dup rs35402411
NM_201590.3(CACNB2):c.*600_*601TA[4] rs72366492
NM_201590.3(CACNB2):c.*608T>A rs4748484
NM_201590.3(CACNB2):c.*609A>T rs4748485
NM_201590.3(CACNB2):c.*70_*71dup rs3841459
NM_201590.3(CACNB2):c.*995T>A rs189039831
NM_201590.3(CACNB2):c.1044+6T>C rs147857449
NM_201590.3(CACNB2):c.1152T>C (p.Asp384=) rs878855310
NM_201590.3(CACNB2):c.1227C>A (p.Ala409=) rs1554842250
NM_201590.3(CACNB2):c.1302C>T (p.Ser434=) rs1060504915
NM_201590.3(CACNB2):c.1349C>T (p.Thr450Ile) rs143326262
NM_201590.3(CACNB2):c.1356C>T (p.Arg452=) rs34813638
NM_201590.3(CACNB2):c.1377T>C (p.Ala459=) rs191856144
NM_201590.3(CACNB2):c.1391A>C (p.Glu464Ala) rs138060429
NM_201590.3(CACNB2):c.1429C>T (p.Arg477Cys) rs202152674
NM_201590.3(CACNB2):c.1430G>A (p.Arg477His) rs184280124
NM_201590.3(CACNB2):c.1526G>A (p.Arg509Gln) rs766377211
NM_201590.3(CACNB2):c.1539C>T (p.Tyr513=) rs2228645
NM_201590.3(CACNB2):c.1614C>A (p.Asp538Glu) rs144182966
NM_201590.3(CACNB2):c.1614C>T (p.Asp538=) rs144182966
NM_201590.3(CACNB2):c.1623C>T (p.His541=) rs61733967
NM_201590.3(CACNB2):c.1632T>C (p.Ser544=) rs34503140
NM_201590.3(CACNB2):c.1635C>T (p.Asp545=) rs1060504914
NM_201590.3(CACNB2):c.1654C>T (p.Arg552Trp) rs61733968
NM_201590.3(CACNB2):c.1671C>T (p.Asp557=) rs777607595
NM_201590.3(CACNB2):c.1752T>C (p.Asp584=) rs1554843214
NM_201590.3(CACNB2):c.1773A>G (p.Lys591=) rs772752419
NM_201590.3(CACNB2):c.1803T>G (p.Asp601Glu) rs58225473
NM_201590.3(CACNB2):c.1813C>T (p.Arg605Cys) rs77141223
NM_201590.3(CACNB2):c.750G>A (p.Leu250=) rs1246608729
NM_201590.3(CACNB2):c.855C>T (p.His285=) rs747015946
NM_201590.3(CACNB2):c.892+7C>T rs4314963

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