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: rs702873
rs702873
3 0.882 0.120 2 60854407 intron variant C/T snv 0.35 0.800 1.000 2 2010 2015
dbSNP: rs62149416
rs62149416
2 0.925 0.040 2 60856371 intron variant T/C snv 0.26 0.800 1.000 1 2012 2012
dbSNP: rs35741374
rs35741374
1 1.000 0.040 2 60845432 intron variant C/T snv 0.64 0.700 1.000 1 2015 2015
dbSNP: rs702872
rs702872
5 0.827 0.120 2 60854175 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs842625
rs842625
1 1.000 0.040 2 60853347 intron variant G/A snv 0.35 0.700 1.000 1 2015 2015