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: rs10795763
rs10795763
2 0.925 0.120 10 6054236 intron variant G/T snv 0.45 0.010 1.000 1 2014 2014
dbSNP: rs11256497
rs11256497
2 0.925 0.120 10 6045831 intron variant G/A snv 0.28 0.010 1.000 1 2014 2014
dbSNP: rs141303532
rs141303532
1 1.000 0.040 17 17221515 missense variant G/A;T snv 1.0E-04; 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs231775
rs231775
115 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs2476491
rs2476491
8 0.776 0.240 10 6053447 intron variant A/T snv 0.25 0.010 1.000 1 2014 2014
dbSNP: rs791587
rs791587
2 0.925 0.120 10 6046736 intron variant A/G snv 0.51 0.010 1.000 1 2014 2014