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: rs17114046
rs17114046
1 0.925 0.040 1 56500678 intron variant A/G snv 0.12 0.800 1.000 2 2011 2011
dbSNP: rs17114036
rs17114036
3 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.800 1.000 1 2011 2014
dbSNP: rs2404715
rs2404715
1 1.000 0.040 1 56543106 intron variant C/T snv 7.6E-02 0.700 1.000 1 2011 2011