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: rs2274223
rs2274223
40 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 0.100 0.923 13 2012 2019
dbSNP: rs3765524
rs3765524
17 0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 0.020 1.000 2 2014 2019
dbSNP: rs10509670
rs10509670
5 0.851 0.080 10 94308190 intron variant A/G snv 0.30 0.010 1.000 1 2019 2019
dbSNP: rs2274224
rs2274224
6 0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44 0.010 1.000 1 2013 2013
dbSNP: rs776933870
rs776933870
3 0.925 0.080 10 94306632 missense variant A/G snv 8.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs7922612
rs7922612
14 0.752 0.080 10 94051682 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014