ClinVar Miner

List of variants in gene ANK2 reported as likely benign by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.9854T>C (p.Ile3285Thr) rs36210417 0.00822
NM_001148.6(ANK2):c.3379+12T>G rs139528815 0.00812
NM_001148.6(ANK2):c.1863C>G (p.Ser621=) rs146425138 0.00089
NM_001148.6(ANK2):c.11493G>T (p.Glu3831Asp) rs144046572 0.00070
NM_001148.6(ANK2):c.11459G>A (p.Arg3820Gln) rs138085317 0.00067
NM_001148.6(ANK2):c.9923C>G (p.Thr3308Ser) rs145145511 0.00051
NM_001148.6(ANK2):c.10289A>C (p.Glu3430Ala) rs149574241 0.00046
NM_001148.6(ANK2):c.2727T>A (p.Thr909=) rs144548535 0.00036
NM_001148.6(ANK2):c.2080-18G>T rs199937888 0.00016
NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg) rs371787039 0.00014
NM_001148.6(ANK2):c.1135C>T (p.Arg379Cys) rs143043717 0.00006
NM_001148.6(ANK2):c.8124A>G (p.Val2708=) rs776586126 0.00006
NM_001148.6(ANK2):c.9936C>T (p.Ser3312=) rs758162927 0.00005
NM_001148.6(ANK2):c.11616C>T (p.Asp3872=) rs768755447 0.00002
NM_001148.6(ANK2):c.9681C>T (p.Thr3227=) rs144466117 0.00002
NM_001148.6(ANK2):c.285+12G>A rs752639381 0.00001
NM_001148.6(ANK2):c.8768A>G (p.Gln2923Arg) rs551454026 0.00001
NM_001148.6(ANK2):c.9555C>T (p.Asp3185=) rs371509239 0.00001
NM_001148.6(ANK2):c.9598C>T (p.Leu3200Phe) rs750774547 0.00001
NM_001148.6(ANK2):c.10362G>T (p.Arg3454Ser) rs55726422

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.