Source: ALL
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: rs16864709
rs16864709 		1 3 152918515 intergenic variant G/T snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs17684427
rs17684427
CADPS2
1 7 122842923 intron variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs362272
rs362272
HTT
2 1.000 0.120 4 3233253 missense variant G/A;T snv 0.29 0.700 1.000 1 2016 2016