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: rs121912585
rs121912585
4 0.851 0.160 12 39332405 missense variant G/A snv 0.800 1.000 4 2003 2014
dbSNP: rs121912586
rs121912586
3 0.882 0.160 12 39332404 missense variant C/T snv 0.800 1.000 4 2003 2014
dbSNP: rs121912587
rs121912587
1 1.000 0.160 12 39332236 missense variant A/G snv 0.800 1.000 4 2003 2014
dbSNP: rs121912588
rs121912588
1 1.000 0.160 12 39358326 missense variant A/G snv 0.800 1.000 4 2003 2014
dbSNP: rs121912589
rs121912589
1 1.000 0.160 12 39332608 missense variant T/C snv 0.800 1.000 4 2003 2014
dbSNP: rs121912590
rs121912590
1 1.000 0.160 12 39332607 missense variant A/C snv 0.800 1.000 4 2003 2014
dbSNP: rs864321718
rs864321718
1 1.000 0.160 12 39370222 missense variant G/A;C snv 4.0E-06 0.700 0