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: rs13245690
rs13245690
3 7 121145010 intron variant A/G snv 0.32 0.700 1.000 2 2012 2017
dbSNP: rs13223036
rs13223036
2 7 121107254 intron variant T/G snv 0.29 0.700 1.000 1 2014 2014
dbSNP: rs2110281
rs2110281
2 7 121085755 intron variant G/A snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs34249834
rs34249834
1 7 121134062 intron variant C/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs35789132
rs35789132
1 7 121163232 intron variant A/G snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs4609139
rs4609139
2 7 121263761 intron variant A/T snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs67991850
rs67991850
1 7 121173866 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs798943
rs798943
2 7 121118845 intron variant G/A snv 0.35 0.700 1.000 1 2014 2014
dbSNP: rs9640799
rs9640799
1 7 121190161 intron variant A/G snv 0.62 0.700 1.000 1 2018 2018