ClinVar Miner

List of variants in gene KCNQ2 reported as uncertain significance for not specified

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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_172107.4(KCNQ2):c.2315C>T (p.Pro772Leu) rs774206764 0.00004
NM_172107.4(KCNQ2):c.2260G>A (p.Ala754Thr) rs773822234 0.00003
NM_172107.4(KCNQ2):c.1394G>A (p.Arg465Gln) rs1459078042 0.00001
NM_172107.4(KCNQ2):c.2000C>T (p.Ala667Val) rs563291132 0.00001
NM_172107.4(KCNQ2):c.2117C>A (p.Ala706Asp) rs980128101 0.00001
NM_172107.4(KCNQ2):c.2234C>T (p.Pro745Leu) rs1057518569 0.00001
NM_172107.4(KCNQ2):c.2332G>A (p.Glu778Lys) rs1264858438 0.00001
NM_172107.4(KCNQ2):c.1057C>T (p.Arg353Cys) rs118192218
NM_172107.4(KCNQ2):c.12G>C (p.Lys4Asn) rs776223064
NM_172107.4(KCNQ2):c.1704C>G (p.Ile568Met) rs144909985
NM_172107.4(KCNQ2):c.2102_2104del (p.Phe701del) rs758334927
NM_172107.4(KCNQ2):c.2138C>T (p.Pro713Leu) rs750333438
NM_172107.4(KCNQ2):c.388-9C>G rs371784719
NM_172107.4(KCNQ2):c.436T>A (p.Trp146Arg) rs1555873982
NM_172107.4(KCNQ2):c.479G>C (p.Arg160Pro) rs1057518323
NM_172107.4(KCNQ2):c.766G>C (p.Gly256Arg) rs1057518500

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