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: rs12156238
rs12156238
FAM167A ; FAM167A-AS1
1 1.000 0.160 8 11427626 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs3179891
rs3179891
LINC02580
1 1.000 0.160 2 43092840 intron variant G/A snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs62137541
rs62137541 		1 1.000 0.160 2 43088349 downstream gene variant T/C snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs62283056
rs62283056
WFS1
3 0.882 0.280 4 6274903 intron variant G/C snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs7562946
rs7562946 		1 1.000 0.160 2 43091570 upstream gene variant A/G snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs7578467
rs7578467 		1 1.000 0.160 2 43088710 downstream gene variant C/A;T snv 0.700 1.000 1 2017 2017