ClinVar Miner

List of variants in gene VARS2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020442.6(VARS2):c.2467-77A>G rs2257347 0.68148
NM_020442.6(VARS2):c.3033C>T (p.Asp1011=) rs1043483 0.66272
NM_020442.6(VARS2):c.2673+184G>A rs2532941 0.63471
NM_020442.6(VARS2):c.-28+82T>C rs1264306 0.52561
NM_020442.6(VARS2):c.1633-106G>A rs2517467 0.50641
NM_020442.6(VARS2):c.1345T>C (p.Trp449Arg) rs2249464 0.50569
NM_020442.6(VARS2):c.168G>T (p.Ala56=) rs1264301 0.28870
NM_020442.6(VARS2):c.671+229A>T rs41268036 0.28809
NM_020442.6(VARS2):c.671+225G>A rs41266876 0.28273
NM_020442.6(VARS2):c.753+70A>C rs1264297 0.27899
NM_020442.6(VARS2):c.672-219A>G rs1264298 0.27891
NM_020442.6(VARS2):c.1288C>T (p.Leu430=) rs2249459 0.27889
NM_020442.6(VARS2):c.985+56A>G rs9262288 0.27886
NM_020442.6(VARS2):c.2785+64C>G rs2532939 0.27883
NM_020442.6(VARS2):c.2893G>A (p.Ala965Thr) rs2252863 0.27881
NM_020442.6(VARS2):c.986-254C>G rs9262293 0.27879
NM_020442.6(VARS2):c.2786-70G>A rs2252856 0.27875
NM_020442.6(VARS2):c.201+42A>G rs1264300 0.27874
NM_020442.6(VARS2):c.985+238G>A rs9262290 0.27871
NM_020442.6(VARS2):c.1075-224C>T rs7756286 0.27870
NM_020442.6(VARS2):c.1632+38A>G rs2532943 0.27869
NM_020442.6(VARS2):c.-28+156C>T rs1264305 0.27868
NM_020442.6(VARS2):c.21C>T (p.Ala7=) rs1264302 0.27868
NM_020442.6(VARS2):c.985+103T>A rs9262289 0.27868
NM_020442.6(VARS2):c.1075-191T>C rs7738138 0.27866
NM_020442.6(VARS2):c.3090+46G>A rs2532938 0.27866
NM_020442.6(VARS2):c.574-9C>T rs1264299 0.27863
NM_020442.6(VARS2):c.2658C>T (p.Pro886=) rs2532942 0.27861
NM_020442.6(VARS2):c.-27-74A>G rs1264303 0.27857
NM_020442.6(VARS2):c.1353G>A (p.Leu451=) rs2517468 0.27814
NM_020442.6(VARS2):c.2750G>A (p.Arg917Gln) rs9394021 0.22711
NM_020442.6(VARS2):c.1272C>T (p.Ser424=) rs2285319 0.22709
NM_020442.6(VARS2):c.2674-51del rs35056976 0.22684
NM_020442.6(VARS2):c.1656T>C (p.Val552=) rs2074511 0.18932
NM_020442.6(VARS2):c.3146G>A (p.Arg1049Gln) rs4678 0.15318
NM_020442.6(VARS2):c.1074+37C>T rs41273021 0.07963
NM_020442.6(VARS2):c.-27-172C>T rs1264304 0.07620
NM_020442.6(VARS2):c.190G>A (p.Gly64Arg) rs6926723 0.06682
NM_020442.6(VARS2):c.76C>T (p.His26Tyr) rs6926224 0.06678
NM_020442.6(VARS2):c.1479+91G>A rs7766094 0.05686
NM_020442.6(VARS2):c.1075-293G>A rs111371873 0.04544
NM_020442.6(VARS2):c.2466+168G>C rs535228401 0.03802
NM_020442.6(VARS2):c.2412C>T (p.Leu804=) rs17189635 0.02324
NM_020442.6(VARS2):c.-27-156C>T rs3218831 0.02126
NM_020442.6(VARS2):c.1074+235G>C rs11757745 0.02076
NM_020442.6(VARS2):c.1514C>T (p.Ser505Phe) rs61746524 0.01404
NM_020442.6(VARS2):c.2578C>T (p.Leu860=) rs116118019 0.01372
NM_020442.6(VARS2):c.1480-9T>C rs116172961 0.00932
NM_020442.6(VARS2):c.1670C>A (p.Ala557Asp) rs55822421 0.00736
NM_020442.6(VARS2):c.423G>A (p.Met141Ile) rs141408930 0.00569
NM_020442.6(VARS2):c.671+174G>A rs146114215 0.00527
NM_020442.6(VARS2):c.2500C>T (p.Arg834Cys) rs142520878 0.00488
NM_020442.6(VARS2):c.607G>A (p.Gly203Arg) rs73430135 0.00342
NM_020442.6(VARS2):c.2467-19C>T rs183366836 0.00212
NM_020442.6(VARS2):c.1166-83_1166-67dup rs9281078
NM_020442.6(VARS2):c.2466+168del rs111876652
NM_020442.6(VARS2):c.2673+255G>C rs2532940
NM_020442.6(VARS2):c.2673+40G>C rs2252760
NM_020442.6(VARS2):c.2961+69del rs34092836
NM_020442.6(VARS2):c.574-42_574-35del rs57637932
NM_020442.6(VARS2):c.671+205GT[13] rs28383826
NM_020442.6(VARS2):c.671+205GT[14] rs28383826
NM_020442.6(VARS2):c.671+219_671+220insGGTG rs371645693
NM_020442.6(VARS2):c.671+227G>A rs9262287
NM_020442.6(VARS2):c.671+231_671+232dup rs9281077
NM_020442.6(VARS2):c.671+232TA[10] rs145049694
NM_020442.6(VARS2):c.985+257TTTG[4] rs147192830

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.