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: rs154774633
rs154774633
2 0.925 0.120 15 68214387 missense variant A/G snv 0.700 1.000 1 2011 2011
dbSNP: rs154774634
rs154774634
1 1.000 0.120 15 68211853 missense variant C/T snv 1.6E-05 2.1E-05 0.700 1.000 1 2011 2011
dbSNP: rs154774635
rs154774635
1 1.000 0.120 15 68218595 missense variant G/A snv 0.700 1.000 1 2011 2011
dbSNP: rs154774636
rs154774636
2 0.925 0.120 15 68229568 missense variant C/G snv 0.700 1.000 1 2011 2011
dbSNP: rs154774638
rs154774638
1 1.000 0.120 15 68211715 missense variant C/T snv 3.2E-05 2.8E-05 0.700 1.000 1 2011 2011
dbSNP: rs154774641
rs154774641
1 1.000 0.120 15 68214356 missense variant G/C;T snv 0.700 1.000 1 2011 2011