List of variants in gene SNTA1 reported as likely benign for Long QT syndrome 12

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.317G>A (p.Arg106Gln)	rs75025585	0.00904
NM_003098.3(SNTA1):c.1426-5T>C	rs183939417	0.00221
NM_003098.3(SNTA1):c.770C>G (p.Ala257Gly)	rs56157422	0.00217
NM_003098.3(SNTA1):c.221C>T (p.Pro74Leu)	rs572545726	0.00198
NM_003098.3(SNTA1):c.993C>T (p.Arg331=)	rs143309917	0.00125
NM_003098.3(SNTA1):c.984C>T (p.Pro328=)	rs138863915	0.00121
NM_003098.3(SNTA1):c.1488C>A (p.Ala496=)	rs34901081	0.00106
NM_003098.3(SNTA1):c.619C>T (p.Arg207Trp)	rs139537086	0.00044
NM_003098.3(SNTA1):c.909+17G>T	rs376695170	0.00021
NM_003098.3(SNTA1):c.1088A>C (p.Glu363Ala)	rs147964932	0.00017
NM_003098.3(SNTA1):c.669G>A (p.Ser223=)	rs199762207
NM_003098.3(SNTA1):c.770C>T (p.Ala257Val)	rs56157422

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