ClinVar Miner

Variants in gene ANK2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 12
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HGVS dbSNP
NM_001148.6(ANK2):c.10861C>G (p.Leu3621Val) rs45570339
NM_001148.6(ANK2):c.10976G>T (p.Arg3659Leu) rs556640912
NM_001148.6(ANK2):c.11032+17G>A rs587780853
NM_001148.6(ANK2):c.11032+19A>G rs200769962
NM_001148.6(ANK2):c.11119G>A (p.Asp3707Asn) rs199549660
NM_001148.6(ANK2):c.11538C>T (p.Leu3846=) rs45602336
NM_001148.6(ANK2):c.11716C>T (p.Arg3906Trp) rs121912706
NM_001148.6(ANK2):c.1773T>C (p.Ser591=) rs374775005
NM_001148.6(ANK2):c.2060A>G (p.Asn687Ser) rs29372
NM_001148.6(ANK2):c.4315G>T (p.Gly1439Cys) rs34591340
NM_001148.6(ANK2):c.9286A>G (p.Ser3096Gly) rs144158934
NM_001148.6(ANK2):c.962G>A (p.Arg321Gln) rs150226540

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