List of variants in gene combination LOC110121288, SCN10A reported as benign for cardiovascular disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_006514.4(SCN10A):c.3218T>C (p.Val1073Ala)	rs6795970	0.70355
NM_006514.4(SCN10A):c.3088-510A>G	rs6801957	0.67159
NM_006514.4(SCN10A):c.3275T>C (p.Leu1092Pro)	rs12632942	0.21722
NM_006514.4(SCN10A):c.3393C>G (p.Thr1131=)	rs6771157	0.21708
NM_006514.4(SCN10A):c.2884A>G (p.Ile962Val)	rs57326399	0.20797
NM_006514.4(SCN10A):c.2937C>T (p.Gly979=)	rs59468016	0.18899
NM_006514.4(SCN10A):c.3192G>A (p.Thr1064=)	rs6791171	0.15667
NM_006514.4(SCN10A):c.3088-20T>C	rs11129804	0.06869
NM_006514.4(SCN10A):c.3133C>A (p.Pro1045Thr)	rs73062575	0.01804
NM_006514.4(SCN10A):c.3087+15C>T	rs140924179	0.00650
NM_006514.4(SCN10A):c.3229-20C>T	rs73825880	0.00248
NM_006514.4(SCN10A):c.3291C>G (p.Ile1097Met)	rs148041371	0.00031
NM_006514.4(SCN10A):c.2814C>T (p.Phe938=)	rs200870389	0.00011
NM_006514.4(SCN10A):c.3238G>A (p.Asp1080Asn)	rs376528831	0.00008
NM_006514.4(SCN10A):c.2850A>G (p.Lys950=)	rs7374804

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