ClinVar Miner

List of variants in gene combination LOC110121269, SCN5A reported as likely benign for Brugada syndrome

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Total variants: 8
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HGVS dbSNP
NM_198056.2(SCN5A):c.2788-6C>T rs41260344
NM_198056.2(SCN5A):c.2976C>T (p.Pro992=) rs193922725
NM_198056.2(SCN5A):c.3006C>G (p.Pro1002=) rs1553699716
NM_198056.2(SCN5A):c.3132C>T (p.Pro1044=) rs547709944
NM_198056.2(SCN5A):c.3183A>G (p.Glu1061=) rs7430407
NM_198056.2(SCN5A):c.3192G>A (p.Glu1064=) rs886039126
NM_198056.2(SCN5A):c.3270G>A (p.Pro1090=) rs752999955
NM_198056.2(SCN5A):c.3308C>A (p.Ser1103Tyr) rs7626962

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