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: rs1441549097
rs1441549097
1 1.000 16 1587222 missense variant A/G snv 8.0E-06 1.4E-05 0.800 1.000 3 2015 2016
dbSNP: rs145549969
rs145549969
1 1.000 16 1525280 missense variant A/G snv 7.0E-06 0.800 1.000 3 2015 2016
dbSNP: rs387907192
rs387907192
2 0.925 0.160 16 1564074 missense variant C/T snv 4.0E-06 3.5E-05 0.800 1.000 3 2015 2016
dbSNP: rs559371453
rs559371453
1 1.000 16 1511137 missense variant A/G snv 8.7E-06 1.4E-05 0.800 1.000 3 2015 2016
dbSNP: rs758052634
rs758052634
1 1.000 16 1580832 missense variant G/A snv 3.2E-05 1.4E-05 0.800 0
dbSNP: rs1555491448
rs1555491448
2 0.925 0.160 16 1584257 missense variant A/G snv 0.700 1.000 3 2015 2016
dbSNP: rs767213195
rs767213195
1 1.000 16 1526044 missense variant G/A snv 1.4E-05 2.8E-05 0.700 1.000 3 2015 2016
dbSNP: rs772757427
rs772757427
1 1.000 16 1602527 missense variant G/A snv 2.0E-05 2.1E-05 0.700 1.000 3 2015 2016
dbSNP: rs781117803
rs781117803
1 1.000 16 1564075 missense variant G/A;C snv 8.0E-06 0.700 1.000 3 2015 2016
dbSNP: rs1555487977
rs1555487977
1 1.000 16 1566161 frameshift variant TATT/- delins 0.700 0
dbSNP: rs200065348
rs200065348
1 1.000 16 1520178 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs200292484
rs200292484
1 1.000 16 1586264 missense variant C/T snv 7.2E-05 5.6E-05 0.700 0
dbSNP: rs376586707
rs376586707
2 0.925 0.160 16 1557934 splice donor variant C/A snv 5.6E-05 5.6E-05 0.700 0
dbSNP: rs745576178
rs745576178
1 1.000 16 1524860 missense variant G/A snv 8.0E-06; 4.0E-06 7.0E-06 0.700 0
dbSNP: rs751323480
rs751323480
1 1.000 16 1557966 missense variant C/G;T snv 2.0E-05 0.700 0
dbSNP: rs770890983
rs770890983
1 1.000 16 1584324 missense variant C/G snv 1.2E-05 0.700 0
dbSNP: rs773372123
rs773372123
5 0.851 0.160 16 1587209 missense variant C/T snv 2.0E-05 0.700 0