List of variants studied for atrial fibrillation, familial, 10 by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.647C>T (p.Ser216Leu)	rs41276525	0.00065
NM_000335.5(SCN5A):c.3875T>C (p.Phe1292Ser)	rs41311127	0.00048
NM_000335.5(SCN5A):c.1340C>G (p.Ala447Gly)	rs199473113	0.00024
NM_000335.5(SCN5A):c.2071G>A (p.Ala691Thr)	rs199473146	0.00012
NM_000335.5(SCN5A):c.3047C>T (p.Thr1016Met)	rs199473185	0.00006
NM_000335.5(SCN5A):c.2314G>A (p.Asp772Asn)	rs199473157	0.00001
NM_000335.5(SCN5A):c.458C>T (p.Pro153Leu)	rs1298498462	0.00001
NM_000335.5(SCN5A):c.65C>T (p.Ala22Val)	rs776925980	0.00001
NM_000335.5(SCN5A):c.1109C>T (p.Thr370Met)	rs199473099
NM_000335.5(SCN5A):c.1794T>C (p.Asn598=)	rs2061958215
NM_000335.5(SCN5A):c.3530G>C (p.Cys1177Ser)	rs1169229420
NM_000335.5(SCN5A):c.3564G>A (p.Lys1188=)	rs1375890695
NM_000335.5(SCN5A):c.3877G>A (p.Ala1293Thr)
NM_000335.5(SCN5A):c.4613G>A (p.Cys1538Tyr)	rs770780069
NM_000335.5(SCN5A):c.5372A>T (p.Asp1791Val)	rs774917987

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