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: rs1131691776
rs1131691776
1 1.000 0.040 2 166199771 missense variant A/G snv 0.810 1.000 1 2015 2015
dbSNP: rs121908910
rs121908910
3 0.882 0.120 2 166272731 missense variant G/A;C snv 1.8E-05; 4.4E-06 0.800 1.000 3 2006 2015
dbSNP: rs121908911
rs121908911
1 1.000 0.040 2 166228971 missense variant A/T snv 0.800 1.000 3 2006 2015
dbSNP: rs121908912
rs121908912
1 1.000 0.040 2 166228972 missense variant C/A snv 0.800 1.000 3 2006 2015
dbSNP: rs121908913
rs121908913
3 0.882 0.120 2 166228969 missense variant C/A snv 0.800 1.000 3 2006 2015
dbSNP: rs121908914
rs121908914
1 1.000 0.040 2 166204448 missense variant A/G;T snv 0.800 1.000 3 2006 2015
dbSNP: rs121908915
rs121908915
1 1.000 0.040 2 166204439 missense variant G/A snv 0.800 1.000 3 2006 2015
dbSNP: rs1553474394
rs1553474394
1 1.000 0.040 2 166204446 missense variant A/C snv 0.800 1.000 3 2006 2015
dbSNP: rs879253994
rs879253994
2 0.925 0.080 2 166199711 missense variant G/A;T snv 4.0E-06 0.800 1.000 3 2006 2015