ClinVar Miner

List of variants in gene ADAR reported as benign for reticulate pigment disorder

Included ClinVar conditions (10):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001111.5(ADAR):c.78G>A (p.Arg26=) rs1802645 0.99723
NM_001111.5(ADAR):c.298A>G (p.Arg100Gly) rs1466731 0.99604
NM_001111.5(ADAR):c.1151A>G (p.Lys384Arg) rs2229857 0.61729
NM_001111.5(ADAR):c.*1016C>T rs1127314 0.59417
NM_001111.5(ADAR):c.*1790A>G rs1127326 0.59410
NM_001111.5(ADAR):c.*619C>T rs1127311 0.41540
NM_001111.5(ADAR):c.*857C>T rs1127313 0.41404
NM_001111.5(ADAR):c.3443+8G>A rs9427094 0.40966
NM_001111.5(ADAR):c.*1242A>C rs1127317 0.29977
NM_001111.5(ADAR):c.*1549T>A rs9616 0.21349
NM_001111.5(ADAR):c.*943C>A rs34167604 0.02238
NM_001111.5(ADAR):c.1760A>G (p.Tyr587Cys) rs17843865 0.01046
NM_001111.5(ADAR):c.*938A>C rs147862510 0.00621
NM_001111.5(ADAR):c.298= (p.Arg100=) rs1466731 0.00396
NM_001111.5(ADAR):c.*413A>T rs115205788 0.00367
NM_001111.5(ADAR):c.*1436G>T rs144500439 0.00255
NM_001111.5(ADAR):c.1003A>T (p.Ile335Phe) rs34154757 0.00235
NM_001111.5(ADAR):c.*2199C>T rs140535856 0.00229
NM_001111.5(ADAR):c.*2033G>A rs571724294 0.00210
NM_001111.5(ADAR):c.2079+8G>A rs376867928 0.00139
NM_001111.5(ADAR):c.1926T>C (p.His642=) rs150171059 0.00135
NM_001111.5(ADAR):c.2886-11_2886-10del rs557801982 0.00128
NM_001111.5(ADAR):c.*2623C>T rs112827019 0.00111
NM_001111.5(ADAR):c.*2643G>A rs539051807 0.00084
NM_001111.5(ADAR):c.*368G>A rs558906089 0.00079
NM_001111.5(ADAR):c.*245T>C rs376176238 0.00077
NM_001111.5(ADAR):c.*898G>A rs140910871 0.00063
NM_001111.5(ADAR):c.3018C>T (p.Asn1006=) rs151241634 0.00063
NM_001111.5(ADAR):c.3523A>C (p.Arg1175=) rs146625055 0.00042
NM_001111.5(ADAR):c.772G>A (p.Gly258Arg) rs201143561 0.00039
NM_001111.5(ADAR):c.1887C>G (p.Ser629=) rs747820726 0.00019
NM_001111.5(ADAR):c.2496+9G>A rs199698434 0.00017
NM_001111.5(ADAR):c.2497-15C>T rs113249520 0.00014
NM_001111.5(ADAR):c.1934+8C>T rs376025865 0.00013
NM_001111.5(ADAR):c.1935-20C>T rs17843867 0.00012
NM_001111.5(ADAR):c.1851C>A (p.Thr617=) rs764879657 0.00009
NM_001111.5(ADAR):c.57C>T (p.Gly19=) rs137983302 0.00006
NM_001111.5(ADAR):c.1934+12G>A rs776357782 0.00005
NM_001111.5(ADAR):c.2319C>T (p.Cys773=) rs750666914 0.00004
NM_001111.5(ADAR):c.1785+5G>A rs17843866 0.00002
NM_001111.5(ADAR):c.*1614T>A rs530015999 0.00001
NM_001111.5(ADAR):c.*25G>C rs780228174 0.00001
NM_001111.5(ADAR):c.1846G>A (p.Val616Ile) rs570647049 0.00001
NM_001111.5(ADAR):c.2496+8C>T rs770464278 0.00001
NM_001111.5(ADAR):c.650G>A (p.Ser217Asn) rs199906332 0.00001
NM_001111.5(ADAR):c.*517AG[1] rs16361
NM_001111.5(ADAR):c.1126G>T (p.Ala376Ser)
NM_001111.5(ADAR):c.1577A>G (p.Gln526Arg) rs770224427
NM_001111.5(ADAR):c.1897C>T (p.Arg633Cys)
NM_001111.5(ADAR):c.2361G>A (p.Ala787=)
NM_001111.5(ADAR):c.2496+35C>G rs7532276
NM_001111.5(ADAR):c.3019+19dup

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.