ClinVar Miner

List of variants in gene combination LOC110121269, SCN5A 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: 21
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HGVS dbSNP
NM_000335.4(SCN5A):c.2788-6C>T rs41260344
NM_000335.4(SCN5A):c.2886C>T (p.Ala962=) rs544057915
NM_000335.4(SCN5A):c.2931C>G (p.Thr977=) rs780713625
NM_000335.4(SCN5A):c.2976C>T (p.Pro992=) rs193922725
NM_000335.4(SCN5A):c.3003G>C (p.Leu1001=) rs758064769
NM_000335.4(SCN5A):c.3006C>G (p.Pro1002=) rs1553699716
NM_000335.4(SCN5A):c.3033G>A (p.Pro1011=) rs764425131
NM_000335.4(SCN5A):c.3057G>A (p.Val1019=) rs372395429
NM_000335.4(SCN5A):c.3068G>A (p.Arg1023His) rs199473592
NM_000335.4(SCN5A):c.3117C>T (p.Pro1039=) rs762151891
NM_000335.4(SCN5A):c.3132C>T (p.Pro1044=) rs547709944
NM_000335.4(SCN5A):c.3168A>C (p.Thr1056=) rs45480800
NM_000335.4(SCN5A):c.3183A>G (p.Glu1061=) rs7430407
NM_000335.4(SCN5A):c.3192G>A (p.Glu1064=) rs886039126
NM_000335.4(SCN5A):c.3207G>A (p.Thr1069=) rs371686822
NM_000335.4(SCN5A):c.3228+6C>G rs368048551
NM_000335.4(SCN5A):c.3259G>A (p.Ala1087Thr) rs369704754
NM_000335.4(SCN5A):c.3267G>A (p.Pro1089=) rs752999955
NM_000335.4(SCN5A):c.3289G>T (p.Val1097Leu) rs199473191
NM_000335.4(SCN5A):c.3305C>A (p.Ser1102Tyr) rs7626962
NM_000335.4(SCN5A):c.3375A>G (p.Pro1125=) rs372328054

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