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: rs3827644
rs3827644
2 0.925 0.080 6 106237320 intron variant G/C snv 0.15 0.800 1.000 1 2013 2013
dbSNP: rs4134466
rs4134466
1 1.000 0.040 6 106129493 intron variant A/G snv 0.70 0.700 1.000 1 2017 2017
dbSNP: rs633724
rs633724
1 1.000 0.040 6 106286165 intron variant C/T snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs802791
rs802791
4 0.851 0.160 6 106121395 intron variant T/C snv 0.75 0.700 1.000 1 2019 2019
dbSNP: rs9373839
rs9373839
3 0.882 0.080 6 106207742 intron variant T/C snv 0.15 0.700 1.000 1 2014 2014