Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1007863
rs1007863
1 1.000 22 43999571 missense variant T/A;C snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs2073080
rs2073080
2 0.925 0.040 22 43998522 intron variant C/T snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs2281292
rs2281292
1 1.000 22 43999509 intron variant A/C snv 0.44 0.47 0.700 1.000 1 2013 2013
dbSNP: rs2401514
rs2401514
1 1.000 22 43998139 intron variant T/A snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs6006473
rs6006473
2 0.925 0.040 22 43997195 intron variant C/T snv 0.47 0.700 1.000 1 2013 2013