List of variants in gene KCNB1 reported as benign for not specified

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004975.4(KCNB1):c.198C>T (p.His66=)	rs520282	0.02665
NM_004975.4(KCNB1):c.2473C>T (p.Pro825Ser)	rs34467662	0.02504
NM_004975.4(KCNB1):c.1847C>G (p.Thr616Ser)	rs2229006	0.01543
NM_004975.4(KCNB1):c.1837C>T (p.Pro613Ser)	rs112735799	0.01273
NM_004975.4(KCNB1):c.2570G>A (p.Ser857Asn)	rs34280195	0.00926
NM_004975.4(KCNB1):c.1182G>A (p.Gly394=)	rs77238446	0.00481
NM_004975.4(KCNB1):c.2334C>T (p.Leu778=)	rs142111310	0.00290
NM_004975.4(KCNB1):c.1389T>A (p.Ile463=)	rs115929614	0.00239
NM_004975.4(KCNB1):c.2106G>A (p.Ala702=)	rs149678923	0.00238
NM_004975.4(KCNB1):c.1296G>A (p.Arg432=)	rs142605642	0.00097
NM_004975.4(KCNB1):c.177G>A (p.Lys59=)	rs117017889	0.00036
NM_004975.4(KCNB1):c.568-18A>G	rs190903326	0.00017
NM_004975.4(KCNB1):c.2396G>A (p.Ser799Asn)	rs1256695300

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