ClinVar Miner

List of variants reported as likely benign for Brugada syndrome 7 by Invitae

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_001040151.2(SCN3B):c.328G>A (p.Val110Ile) rs147205617 0.00029
NM_001040151.2(SCN3B):c.327C>T (p.Asn109=) rs199937307 0.00025
NM_001040151.2(SCN3B):c.93G>A (p.Ser31=) rs753258598 0.00011
NM_001040151.2(SCN3B):c.105C>T (p.Ala35=) rs368979661 0.00010
NM_001040151.2(SCN3B):c.339C>T (p.Asn113=) rs142613556 0.00008
NM_001040151.2(SCN3B):c.585-4A>G rs745830643 0.00008
NM_001040151.2(SCN3B):c.174G>A (p.Thr58=) rs201049075 0.00006
NM_001040151.2(SCN3B):c.570A>G (p.Ala190=) rs575419664 0.00005
NM_001040151.2(SCN3B):c.99G>A (p.Thr33=) rs754476318 0.00004
NM_001040151.2(SCN3B):c.630G>A (p.Ala210=) rs758915355 0.00003
NM_001040151.2(SCN3B):c.445+8T>C rs759996960 0.00002
NM_001040151.2(SCN3B):c.561C>T (p.Ala187=) rs746888620 0.00002
NM_001040151.2(SCN3B):c.309G>A (p.Val103=) rs775194985 0.00001
NM_001040151.2(SCN3B):c.396G>T (p.Arg132=) rs752593287 0.00001
NM_001040151.2(SCN3B):c.55+7A>G rs1057522984 0.00001
NM_001040151.2(SCN3B):c.66C>T (p.Cys22=) rs1487947786 0.00001
NM_001040151.2(SCN3B):c.6T>C (p.Pro2=) rs769826959 0.00001
NM_001040151.2(SCN3B):c.111G>A (p.Gln37=) rs2137247053
NM_001040151.2(SCN3B):c.135C>T (p.Cys45=)
NM_001040151.2(SCN3B):c.192C>T (p.Tyr64=)
NM_001040151.2(SCN3B):c.198C>A (p.Pro66=) rs115752338
NM_001040151.2(SCN3B):c.225C>T (p.Tyr75=)
NM_001040151.2(SCN3B):c.240C>T (p.Gly80=)
NM_001040151.2(SCN3B):c.258C>T (p.Ser86=)
NM_001040151.2(SCN3B):c.27C>T (p.Pro9=)
NM_001040151.2(SCN3B):c.39C>T (p.Leu13=)
NM_001040151.2(SCN3B):c.411G>A (p.Thr137=)
NM_001040151.2(SCN3B):c.423C>T (p.Ile141=) rs879253730
NM_001040151.2(SCN3B):c.445+20T>G
NM_001040151.2(SCN3B):c.446-7C>G rs527845801
NM_001040151.2(SCN3B):c.519G>T (p.Leu173=)
NM_001040151.2(SCN3B):c.525C>T (p.Ile175=)
NM_001040151.2(SCN3B):c.55+11G>A
NM_001040151.2(SCN3B):c.584+9A>C rs2137235766
NM_001040151.2(SCN3B):c.585-16C>T rs2137231130
NM_001040151.2(SCN3B):c.624C>T (p.Asn208=)

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