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: rs10207628
rs10207628
BIN1
2 0.925 0.120 2 127094445 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10994278
rs10994278
ANK3
1 1.000 0.080 10 60249461 intron variant T/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs157582
rs157582
TOMM40
8 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 0.700 1.000 1 2012 2012
dbSNP: rs3849810
rs3849810 		1 1.000 0.080 8 52097046 intergenic variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4038131
rs4038131
VSNL1
2 0.925 0.120 2 17593765 intron variant A/G snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs4576506
rs4576506 		2 0.925 0.120 9 31546474 intergenic variant A/G snv 0.91 0.700 1.000 1 2012 2012
dbSNP: rs549656827
rs549656827 		1 1.000 0.080 5 35349326 intergenic variant G/A snv 6.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs753129
rs753129 		2 0.925 0.120 4 55802265 downstream gene variant A/G snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs75459873
rs75459873 		1 1.000 0.080 1 23929822 downstream gene variant G/A snv 3.2E-02 0.700 1.000 1 2019 2019