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: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2016 2016
dbSNP: rs2525776
rs2525776 		2 0.925 0.080 7 81272303 intergenic variant C/T snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs6714710
rs6714710
ZAP70
2 0.925 0.080 2 97728623 intron variant T/G snv 0.52 0.700 1.000 1 2016 2016
dbSNP: rs72907046
rs72907046 		2 0.925 0.080 6 81418166 intergenic variant A/G snv 8.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs76854344
rs76854344 		2 0.925 0.080 2 123995579 intergenic variant G/T snv 8.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs5848
rs5848
GRN ; FAM171A2
17 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2016 2016
dbSNP: rs63750869
rs63750869
MAPT
6 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.010 1.000 1 2014 2014
dbSNP: rs769265539
rs769265539
PSEN1
1 1.000 14 73192725 missense variant G/A snv 4.0E-06 0.010 1.000 1 2013 2013