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: rs1039559
rs1039559
2 1.000 0.080 4 38829975 intron variant G/A snv 0.62 0.700 1.000 1 2013 2013
dbSNP: rs148906978
rs148906978
2 1.000 0.080 4 38852748 intron variant C/T snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs2174284
rs2174284
1 4 38857718 upstream gene variant C/T snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs5743788
rs5743788
1 4 38831586 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs5743794
rs5743794
1 4 38831106 intron variant C/T snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs5743810
rs5743810
21 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 0.700 1.000 1 2013 2013
dbSNP: rs6531672
rs6531672
1 4 38845390 intron variant T/C snv 0.62 0.700 1.000 1 2013 2013
dbSNP: rs6531673
rs6531673
1 4 38846296 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs7665774
rs7665774
1 4 38842128 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs7673348
rs7673348
1 4 38843577 intron variant G/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs7681628
rs7681628
1 4 38854763 intron variant G/A snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs7687447
rs7687447
1 4 38845358 intron variant C/G;T snv 0.700 1.000 1 2013 2013