List of variants in gene SCN5A reported as likely benign for Sick sinus syndrome 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.5454T>C (p.Asp1818=)	rs1805126	0.44288
NM_000335.5(SCN5A):c.1673A>G (p.His558Arg)	rs1805124	0.24768
NM_000335.5(SCN5A):c.1141-3C>A	rs41312433	0.16821
NM_000335.5(SCN5A):c.100C>T (p.Arg34Cys)	rs6791924	0.03086
NM_000335.5(SCN5A):c.1587T>C (p.Ile529=)	rs45624133	0.00575
NM_000335.5(SCN5A):c.717C>T (p.Ile239=)	rs41285129	0.00407
NM_000335.5(SCN5A):c.2436+12G>A	rs41312419	0.00284
NM_000335.5(SCN5A):c.1890+14G>A	rs145427253	0.00252
NM_000335.5(SCN5A):c.1681C>T (p.Leu561=)	rs45522138	0.00196
NM_000335.5(SCN5A):c.*677G>A	rs45458203	0.00177
NM_000335.5(SCN5A):c.3388-7T>C	rs41310769	0.00009
NM_000335.5(SCN5A):c.5333C>T (p.Thr1778Met)	rs199473634	0.00008
NM_000335.5(SCN5A):c.6000C>T (p.Leu2000=)	rs538707712	0.00001
NM_000335.5(SCN5A):c.1715C>A (p.Ala572Asp)	rs36210423

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