ClinVar Miner

List of variants in gene KCNV2 reported as likely benign by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_133497.4(KCNV2):c.*262T>A rs57109373 0.08241
NM_133497.4(KCNV2):c.*308T>G rs60723920 0.01938
NM_133497.4(KCNV2):c.291C>T (p.Ser97=) rs113456345 0.00237
NM_133497.4(KCNV2):c.1308G>A (p.Val436=) rs139581747 0.00225
NM_133497.4(KCNV2):c.1026C>T (p.Ala342=) rs141789289 0.00222
NM_133497.4(KCNV2):c.1607A>G (p.Asn536Ser) rs77811928 0.00165
NM_133497.4(KCNV2):c.-111C>T rs188986938 0.00158
NM_133497.4(KCNV2):c.612G>A (p.Glu204=) rs186159326 0.00123
NM_133497.4(KCNV2):c.*170A>G rs10967769 0.00094
NM_133497.4(KCNV2):c.957G>A (p.Leu319=) rs141378856 0.00053
NM_133497.4(KCNV2):c.645G>C (p.Lys215Asn) rs201327014 0.00035
NM_133497.4(KCNV2):c.-145T>C rs528809457 0.00024
NM_133497.4(KCNV2):c.1063T>C (p.Phe355Leu) rs75645675
NM_133497.4(KCNV2):c.389C>T (p.Thr130Ile) rs541196988

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