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: rs61295588
rs61295588
2 0.925 0.160 1 156134809 missense variant T/C snv 0.700 1.000 3 2013 2017
dbSNP: rs1057515421
rs1057515421
2 0.925 0.120 1 156136284 stop gained C/T snv 0.700 1.000 2 1999 2016
dbSNP: rs150793926
rs150793926
1 1.000 0.040 2 151924550 intron variant TA/-;TATA;TATATA delins 0.700 1.000 1 2018 2018
dbSNP: rs1846594
rs1846594
2 0.925 0.120 3 113197356 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4341082
rs4341082
1 1.000 0.040 7 142060046 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6556795
rs6556795
1 1.000 0.040 5 165040486 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs74676849
rs74676849
1 1.000 0.040 7 11849866 intergenic variant A/G snv 2.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs11575937
rs11575937
29 0.653 0.480 1 156136985 missense variant G/A;T snv 0.700 0
dbSNP: rs1165819867
rs1165819867
1 1.000 0.040 1 156134892 missense variant G/A;T snv 0.700 0
dbSNP: rs1553265180
rs1553265180
1 1.000 0.040 1 156134500 missense variant T/A;G snv 0.700 0
dbSNP: rs1553265736
rs1553265736
4 0.925 0.040 1 156136080 missense variant G/C snv 0.700 0
dbSNP: rs1553265739
rs1553265739
1 1.000 0.040 1 156136081 missense variant A/T snv 0.700 0
dbSNP: rs1553974835
rs1553974835
2 1.000 0.040 4 173529091 stop gained C/A snv 0.700 0
dbSNP: rs267607581
rs267607581
4 0.925 0.080 1 156137651 splice region variant C/G snv 0.700 0
dbSNP: rs386134243
rs386134243
16 0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs397517889
rs397517889
3 0.925 0.120 1 156136093 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs56771886
rs56771886
2 0.925 0.160 1 156135923 frameshift variant T/- delins 0.700 0
dbSNP: rs57077886
rs57077886
9 0.776 0.240 1 156114947 missense variant C/T snv 0.700 0
dbSNP: rs58362413
rs58362413
2 0.925 0.160 1 156137183 stop gained G/A;C snv 0.700 0
dbSNP: rs58672172
rs58672172
3 0.882 0.160 1 156136251 missense variant C/T snv 1.2E-05 1.4E-05 0.700 0
dbSNP: rs59332535
rs59332535
5 0.827 0.160 1 156134911 missense variant G/A snv 0.700 0
dbSNP: rs59684335
rs59684335
3 0.882 0.120 1 156135280 frameshift variant CT/- delins 0.700 0
dbSNP: rs730882262
rs730882262
4 0.851 0.160 1 156135293 missense variant T/C;G snv 0.700 0
dbSNP: rs863224899
rs863224899
2 0.925 0.080 11 47337580 splice acceptor variant C/T snv 0.700 0
dbSNP: rs104893823
rs104893823
5 0.882 0.040 3 52451285 missense variant C/T snv 0.040 1.000 4 2007 2016