ClinVar Miner

List of variants in gene P2RX2 reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_170682.4(P2RX2):c.468T>C (p.Thr156=) rs7964634 0.67274
NM_170682.4(P2RX2):c.636-13G>A rs6560891 0.66828
NM_170682.4(P2RX2):c.9C>T (p.Ala3=) rs186684886 0.02469
NM_170682.4(P2RX2):c.554+14C>A rs151253585 0.01337
NM_170682.4(P2RX2):c.1302G>A (p.Pro434=) rs114276183 0.01262
NM_170682.4(P2RX2):c.186C>T (p.Ile62=) rs75585377 0.01034
NM_170682.4(P2RX2):c.174-4G>T rs200811971 0.00818
NM_170682.4(P2RX2):c.699C>T (p.Asp233=) rs113782309 0.00585
NM_170682.4(P2RX2):c.1332T>A (p.Pro444=) rs116834114 0.00302
NM_170682.4(P2RX2):c.831G>A (p.Ser277=) rs114365804 0.00190
NM_170682.4(P2RX2):c.774+7C>G rs199743808 0.00186
NM_170682.4(P2RX2):c.211G>A (p.Glu71Lys) rs143664462 0.00163
NM_170682.4(P2RX2):c.491A>G (p.Gln164Arg) rs142844880 0.00097
NM_170682.4(P2RX2):c.1176T>C (p.Pro392=) rs189869132 0.00044
NM_170682.4(P2RX2):c.381+2T>C rs200978001 0.00022
NM_170682.4(P2RX2):c.1363G>A (p.Glu455Lys) rs199955493 0.00020
NM_170682.4(P2RX2):c.762G>A (p.Glu254=) rs144300117 0.00013
NM_170682.4(P2RX2):c.1219G>A (p.Gly407Ser) rs199712315 0.00008
NM_170682.4(P2RX2):c.964G>A (p.Gly322Arg) rs201474543 0.00008
NM_170682.4(P2RX2):c.943C>T (p.Arg315Cys) rs761180947 0.00007
NM_170682.4(P2RX2):c.1234G>C (p.Asp412His) rs374200273 0.00003
NM_170682.4(P2RX2):c.1310G>A (p.Arg437Gln) rs115260724 0.00003
NM_170682.4(P2RX2):c.906-13G>A rs757748091 0.00002
NM_170682.4(P2RX2):c.1090C>G (p.Leu364Val) rs749812549 0.00001
NM_170682.4(P2RX2):c.1413C>T (p.Leu471=) rs568364905 0.00001
NM_170682.4(P2RX2):c.1015A>T (p.Ile339Phe) rs1555299483
NM_170682.4(P2RX2):c.1257A>C (p.Ser419=) rs876657561
NM_170682.4(P2RX2):c.1325_1335del (p.Ile441_Ser442insTer) rs876657423
NM_170682.4(P2RX2):c.457+9G>A rs200457240
NM_170682.4(P2RX2):c.698A>G (p.Asp233Gly) rs1593676004
NM_170682.4(P2RX2):c.775-8_775-6del rs876657424
NM_170682.4(P2RX2):c.800A>G (p.Asn267Ser) rs1555299075
NM_170682.4(P2RX2):c.910G>A (p.Ala304Thr) rs1555299245

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.