List of variants in gene KCNQ1 reported as likely benign for Jervell and Lange-Nielsen syndrome 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP
NM_000218.3(KCNQ1):c.*632C>T
NM_000218.3(KCNQ1):c.1110G>A (p.Ala370=)	rs1805118
NM_000218.3(KCNQ1):c.1179G>T (p.Lys393Asn)	rs12720457
NM_000218.3(KCNQ1):c.1222C>G (p.Pro408Ala)	rs28730756
NM_000218.3(KCNQ1):c.1794+11G>A	rs186188610
NM_000218.3(KCNQ1):c.1927G>A (p.Gly643Ser)	rs1800172
NM_000218.3(KCNQ1):c.207G>T (p.Ala69=)	rs587781009
NM_000218.3(KCNQ1):c.435C>T (p.Ile145=)	rs1800170
NM_000218.3(KCNQ1):c.513C>T (p.Tyr171=)	rs139042529
NM_000218.3(KCNQ1):c.567G>T (p.Gly189=)	rs200669271
NM_000218.3(KCNQ1):c.720C>T (p.His240=)	rs28730754
NM_181798.1(KCNQ1):c.*464G>A	rs141960532
NM_181798.1(KCNQ1):c.*731G>A	rs146324627
NM_181798.1(KCNQ1):c.*806C>T	rs539398869
NM_181798.1(KCNQ1):c.*975C>T	rs74048340
NM_181798.1(KCNQ1):c.1494C>T (p.Pro498=)	rs112113213
NM_181798.1(KCNQ1):c.591C>T (p.Val197=)	rs554518844

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