List of variants in gene KCNA2 reported as likely pathogenic for not provided

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004974.4(KCNA2):c.1013G>A (p.Gly338Glu)	rs1553181301
NM_004974.4(KCNA2):c.1084C>G (p.Pro362Ala)	rs1131691974
NM_004974.4(KCNA2):c.1135G>C (p.Asp379His)	rs2101397006
NM_004974.4(KCNA2):c.1208C>T (p.Ala403Val)	rs1649457143
NM_004974.4(KCNA2):c.1219C>G (p.Pro407Ala)	rs1557731896
NM_004974.4(KCNA2):c.1265_1266del (p.Glu422fs)	rs1064796294
NM_004974.4(KCNA2):c.217C>T (p.Arg73Ter)	rs1570753974
NM_004974.4(KCNA2):c.547G>A (p.Glu183Lys)	rs1553181398
NM_004974.4(KCNA2):c.881G>A (p.Arg294His)	rs886041761
NM_004974.4(KCNA2):c.989T>G (p.Leu330Arg)	rs1057523703

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