List of variants reported as uncertain significance for Jervell and Lange-Nielsen syndrome 1

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

Total variants: 61

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HGVS	dbSNP
NM_000218.2(KCNQ1):c.-38C>T	rs886048160
NM_000218.2(KCNQ1):c.-69G>A	rs886048159
NM_000218.2(KCNQ1):c.386+14C>T	rs370023636
NM_000218.3(KCNQ1):c.*125C>T
NM_000218.3(KCNQ1):c.*240C>T
NM_000218.3(KCNQ1):c.*290A>G
NM_000218.3(KCNQ1):c.*295G>A
NM_000218.3(KCNQ1):c.*66C>T
NM_000218.3(KCNQ1):c.*730C>T
NM_000218.3(KCNQ1):c.*81C>T
NM_000218.3(KCNQ1):c.-55G>C
NM_000218.3(KCNQ1):c.-5T>C	rs532941548
NM_000218.3(KCNQ1):c.1394-13A>G
NM_000218.3(KCNQ1):c.1394-8C>T	rs371488379
NM_000218.3(KCNQ1):c.1590+13C>A
NM_000218.3(KCNQ1):c.1800G>A (p.Thr600=)	rs147091980
NM_000218.3(KCNQ1):c.1830C>T (p.Thr610=)	rs774101297
NM_000218.3(KCNQ1):c.187C>A (p.Pro63Thr)
NM_000218.3(KCNQ1):c.1895G>A (p.Arg632Lys)
NM_000218.3(KCNQ1):c.1903G>A (p.Gly635Arg)	rs199473484
NM_000218.3(KCNQ1):c.387-12C>T
NM_000218.3(KCNQ1):c.41G>T (p.Arg14Leu)	rs1424013094
NM_000218.3(KCNQ1):c.459G>A (p.Thr153=)	rs148121889
NM_000218.3(KCNQ1):c.534C>T (p.Ala178=)
NM_000218.3(KCNQ1):c.684-15C>G
NM_000218.3(KCNQ1):c.780+12G>A
NM_000218.3(KCNQ1):c.811C>T (p.Leu271=)	rs189991547
NM_000218.3(KCNQ1):c.820A>G (p.Ile274Val)	rs199472728
NM_000218.3(KCNQ1):c.868G>A (p.Glu290Lys)	rs199473464
NM_000218.3(KCNQ1):c.900A>C (p.Ala300=)	rs727504769
NM_000218.3(KCNQ1):c.921+12A>G
NM_181798.1(KCNQ1):c.*1025G>C	rs181226788
NM_181798.1(KCNQ1):c.*1055C>T	rs375155898
NM_181798.1(KCNQ1):c.*1088G>C	rs886048177
NM_181798.1(KCNQ1):c.*171G>A	rs886048168
NM_181798.1(KCNQ1):c.*266G>A	rs113029000
NM_181798.1(KCNQ1):c.*391G>A	rs774059974
NM_181798.1(KCNQ1):c.*392A>C	rs868129989
NM_181798.1(KCNQ1):c.*47A>C	rs754931159
NM_181798.1(KCNQ1):c.*539G>C	rs886048171
NM_181798.1(KCNQ1):c.*581T>C	rs765566577
NM_181798.1(KCNQ1):c.*633G>A	rs886048173
NM_181798.1(KCNQ1):c.*652G>A	rs886048174
NM_181798.1(KCNQ1):c.*712G>A	rs745447199
NM_181798.1(KCNQ1):c.*717T>G	rs189162344
NM_181798.1(KCNQ1):c.*837G>A	rs139633955
NM_181798.1(KCNQ1):c.*877C>G	rs763163556
NM_181798.1(KCNQ1):c.*904T>C	rs186055804
NM_181798.1(KCNQ1):c.1095A>G (p.Glu365=)	rs370676650
NM_181798.1(KCNQ1):c.1133+9C>T	rs770840921
NM_181798.1(KCNQ1):c.1175G>A (p.Arg392His)	rs199472788
NM_181798.1(KCNQ1):c.133G>A (p.Val45Met)	rs199472694
NM_181798.1(KCNQ1):c.1413+12C>T	rs727505084
NM_181798.1(KCNQ1):c.1474T>A (p.Leu492Met)	rs199472819
NM_181798.1(KCNQ1):c.267C>A (p.Gly89=)	rs146350010
NM_181798.1(KCNQ1):c.517G>A (p.Ala173Thr)	rs120074187
NM_181798.1(KCNQ1):c.6-7C>T	rs201682200
NM_181798.1(KCNQ1):c.771C>T (p.Ala257=)	rs144615901
NM_181798.1(KCNQ1):c.962C>T (p.Pro321Leu)	rs12720449
NM_181798.1(KCNQ1):c.971G>A (p.Arg324Gln)	rs199472781
NM_181798.1(KCNQ1):c.994G>A (p.Asp332Asn)	rs747704276

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