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: rs1057519964
rs1057519964
1 1.000 0.080 17 49619282 missense variant A/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519965
rs1057519965
1 1.000 0.080 17 49619280 missense variant G/A;C snv 8.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs1057519966
rs1057519966
3 0.882 0.080 17 49619064 missense variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519967
rs1057519967
1 1.000 0.080 17 49619063 missense variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519968
rs1057519968
2 0.925 0.120 17 49619070 missense variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519969
rs1057519969
2 0.925 0.120 17 49619069 missense variant C/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519970
rs1057519970
2 0.925 0.120 17 49619068 missense variant C/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519971
rs1057519971
2 1.000 0.080 17 49619326 missense variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519972
rs1057519972
3 0.882 0.080 17 49619327 missense variant A/T snv 0.700 1.000 1 2016 2016
dbSNP: rs193920894
rs193920894
2 0.925 0.080 17 49619281 missense variant A/C snv 0.700 1.000 1 2016 2016
dbSNP: rs193921065
rs193921065
1 1.000 0.080 17 49619062 missense variant G/C snv 4.0E-06 0.700 1.000 1 2016 2016