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: rs12938031
rs12938031
6 0.851 0.160 17 45777136 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs7207400
rs7207400
2 1.000 0.040 17 45746994 intron variant T/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs7220839
rs7220839
1 1.000 0.040 17 45737779 intron variant C/T snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs110402
rs110402
12 0.790 0.120 17 45802681 intron variant G/A;C snv 0.020 1.000 2 2013 2019
dbSNP: rs17689918
rs17689918
6 0.851 0.080 17 45832722 intron variant G/A snv 0.15 0.010 1.000 1 2016 2016
dbSNP: rs7209436
rs7209436
5 0.851 0.200 17 45792776 intron variant C/T snv 0.43 0.010 1.000 1 2013 2013