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: rs1010022
rs1010022
1 1.000 22 43940430 intron variant A/G snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs11090617
rs11090617
1 1.000 22 43930820 intron variant C/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs1474745
rs1474745
1 1.000 22 43953356 intron variant T/C snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs1883349
rs1883349
1 1.000 22 43936063 intron variant G/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs1883350
rs1883350
1 1.000 22 43932163 intron variant T/C snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs2072905
rs2072905
1 1.000 22 43937599 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2073079
rs2073079
1 1.000 22 43989714 intron variant A/G snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs2073081
rs2073081
1 1.000 22 43939864 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs2228530
rs2228530
1 1.000 2 28778825 missense variant A/C;G snv 0.010 1.000 1 2018 2018
dbSNP: rs2235777
rs2235777
1 1.000 22 43982929 intron variant C/T snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs2235778
rs2235778
1 1.000 22 43993634 intron variant T/C snv 0.48 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: rs2281298
rs2281298
1 1.000 22 43995354 intron variant G/A snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs2294916
rs2294916
1 1.000 22 43945042 intron variant T/G snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs2294922
rs2294922
1 1.000 22 43983685 intron variant G/C snv 0.30 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: rs3788604
rs3788604
1 1.000 22 43992537 intron variant A/G snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs3827385
rs3827385
1 1.000 22 43992937 intron variant T/C snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs4674344
rs4674344
1 1.000 2 218805152 intron variant A/T snv 0.53 0.010 1.000 1 2018 2018
dbSNP: rs4823179
rs4823179
1 1.000 22 43945313 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs6006468
rs6006468
1 1.000 22 43987552 non coding transcript exon variant G/C snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs6006469
rs6006469
1 1.000 22 43987737 non coding transcript exon variant C/G snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs6006602
rs6006602
1 1.000 22 43987520 non coding transcript exon variant C/T snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs926633
rs926633
1 1.000 22 43941653 intron variant G/A snv 0.20 0.700 1.000 1 2013 2013