ClinVar Miner

Variants in gene combination ANK2, LOC126807137 with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 17
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.7106T>C (p.Val2369Ala) rs28377576 0.12654
NM_001148.6(ANK2):c.7831T>C (p.Tyr2611His) rs35338364 0.00539
NM_001148.6(ANK2):c.7132G>A (p.Glu2378Lys) rs141191319 0.00222
NM_001148.6(ANK2):c.7902G>A (p.Val2634=) rs150878494 0.00138
NM_001148.6(ANK2):c.6906C>T (p.Thr2302=) rs139910215 0.00133
NM_001148.6(ANK2):c.7059A>G (p.Gln2353=) rs145782226 0.00124
NM_001148.6(ANK2):c.6912T>C (p.Thr2304=) rs190680846 0.00058
NM_001148.6(ANK2):c.7971C>T (p.Ser2657=) rs146085234 0.00051
NM_001148.6(ANK2):c.7267G>A (p.Ala2423Thr) rs3733616 0.00038
NM_001148.6(ANK2):c.7488A>G (p.Thr2496=) rs143161930 0.00031
NM_001148.6(ANK2):c.7707A>G (p.Ala2569=) rs144407821 0.00026
NM_001148.6(ANK2):c.7251T>C (p.Asp2417=) rs201688836 0.00016
NM_001148.6(ANK2):c.7117A>G (p.Thr2373Ala) rs184514058 0.00012
NM_001148.6(ANK2):c.7131C>T (p.Asp2377=) rs553324580 0.00008
NM_001148.6(ANK2):c.7932G>A (p.Glu2644=) rs201645638 0.00006
NM_001148.6(ANK2):c.7320C>T (p.Ser2440=) rs190590036 0.00005
NM_001148.6(ANK2):c.7943G>A (p.Gly2648Asp) rs563254150 0.00001

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