ClinVar Miner

List of variants studied for atrial fibrillation, familial, 4 by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_172201.2(KCNE2):c.-13+5G>A rs786205806 0.00043
NM_172201.2(KCNE2):c.346G>A (p.Ala116Thr) rs150790888 0.00009
NM_172201.2(KCNE2):c.369_370del (p.Ter124IleextTer?) rs45610936 0.00009
NM_172201.2(KCNE2):c.*234G>A rs981526333 0.00004
NM_172201.2(KCNE2):c.228A>G (p.Arg76=) rs202169020 0.00004
NM_172201.2(KCNE2):c.229C>T (p.Arg77Trp) rs141423405 0.00004
NM_172201.2(KCNE2):c.67A>T (p.Met23Leu) rs747045005 0.00004
NM_172201.2(KCNE2):c.-121C>T rs188625398 0.00003
NM_172201.2(KCNE2):c.204G>A (p.Leu68=) rs200403369 0.00002
NM_172201.2(KCNE2):c.144dup (p.Val49fs) rs751276927 0.00001
NM_172201.2(KCNE2):c.17A>G (p.Asn6Ser) rs776661633 0.00001
NM_172201.2(KCNE2):c.242A>G (p.Asn81Ser) rs1434304789 0.00001
NM_172201.2(KCNE2):c.2T>C (p.Met1Thr) rs867658122 0.00001
NM_172201.2(KCNE2):c.13T>C (p.Ser5Pro) rs2123423458
NM_172201.2(KCNE2):c.193G>C (p.Val65Leu) rs199473364

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