List of variants reported as benign for Benign Neonatal Epilepsy by Illumina Laboratory Services, Illumina

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

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_004519.4(KCNQ3):c.*3597G>A	rs1025436	0.82601
NM_004519.4(KCNQ3):c.*3977G>A	rs2469628	0.43479
NM_004519.4(KCNQ3):c.*3032A>G	rs2469626	0.42325
NM_004519.4(KCNQ3):c.*6812A>G	rs7815106	0.26027
NM_004519.4(KCNQ3):c.*6238T>C	rs10108362	0.25327
NM_004519.4(KCNQ3):c.*426C>G	rs10956640	0.24245
NM_004519.4(KCNQ3):c.*425C>A	rs10956641	0.24242
NM_004519.4(KCNQ3):c.*6340G>A	rs2469629	0.21022
NM_004519.4(KCNQ3):c.*6956A>G	rs2469630	0.20752
NM_004519.4(KCNQ3):c.*8148G>A	rs1437822	0.20680
NM_004519.4(KCNQ3):c.*5932A>C	rs2436130	0.20676
NM_004519.4(KCNQ3):c.*7075A>G	rs2436127	0.20581
NM_004519.4(KCNQ3):c.*7033T>C	rs2436128	0.20576
NM_004519.4(KCNQ3):c.*2137C>T	rs2272679	0.08712
NM_004519.4(KCNQ3):c.1241A>G (p.Glu414Gly)	rs2303995	0.02242
NM_004519.4(KCNQ3):c.*1407A>C	rs76570743	0.02131
NM_004519.4(KCNQ3):c.*4982A>T	rs545252668	0.00007
NM_004519.4(KCNQ3):c.*4243A>T	rs2436131
NM_004519.4(KCNQ3):c.4746_4747insACAG	rs112550767
NM_004519.4(KCNQ3):c.*4982del	rs35772668
NM_004519.4(KCNQ3):c.-142G>T	rs28606540

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