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: rs10980800
rs10980800
2 9 111153625 intron variant T/C snp 0.21 0.800 3 2011 2017
dbSNP: rs12075
rs12075
8 1.000 0.071 1 159205564 missense variant G/A snp 0.51 0.64 0.800 3 2011 2017
dbSNP: rs9880192
rs9880192
4 3 128578726 intergenic variant G/C snp 0.31 0.800 3 2011 2017
dbSNP: rs1449263
rs1449263
4 1.000 0.071 2 181454574 intergenic variant C/T snp 0.56 0.800 2 2011 2014
dbSNP: rs2814778
rs2814778
13 0.878 0.036 1 159204893 5 prime UTR variant T/C snp 0.23 0.800 2 2012 2017
dbSNP: rs445
rs445
8 7 92779056 intron variant C/T snp 0.13 0.800 2 2011 2017
dbSNP: rs10098310
rs10098310
2 8 129601368 G/A,T snp 0.54 0.800 1 2011 2011
dbSNP: rs2124440
rs2124440
2 2 181463487 intron variant G/A snp 0.55 0.700 3 2013 2017
dbSNP: rs1991866
rs1991866
3 8 129611859 intron variant G/A,C snp 0.56 0.700 2 2014 2017
dbSNP: rs2228467
rs2228467
6 1.000 0.071 3 42864624 missense variant T/C snp 5.1E-02 4.9E-02 0.700 2 2013 2017
dbSNP: rs3095254
rs3095254
3 6 31253891 intergenic variant C/G snp 0.56 0.700 2 2011 2014
dbSNP: rs76428106
rs76428106
3 13 28029870 intron variant T/C,G snp 1.0E-02; 9.6E-05 0.700 2 2017 2017
dbSNP: rs1006310
rs1006310
2 1 161841765 intron variant T/C,G snp 0.49 0.700 1 2011 2011
dbSNP: rs10120452
rs10120452
2 9 98623959 intron variant G/A snp 0.17 0.700 1 2011 2011
dbSNP: rs10147992
rs10147992
3 14 25034593 intron variant A/G,T snp 0.49 0.700 1 2011 2011
dbSNP: rs10158210
rs10158210
2 1 158342195 intergenic variant A/G,T snp 0.40 0.700 1 2011 2011
dbSNP: rs10168795
rs10168795
2 2 224888625 intron variant A/G snp 0.24 0.700 1 2017 2017
dbSNP: rs10178249
rs10178249
2 2 124696819 intron variant A/G snp 0.40 0.700 1 2011 2011
dbSNP: rs1037171
rs1037171
2 17 74706839 intron variant G/A snp 0.54 0.700 1 2017 2017
dbSNP: rs10411936
rs10411936
4 1.000 0.071 19 16437564 intron variant A/G snp 0.62 0.700 1 2011 2011
dbSNP: rs10418046
rs10418046
2 19 53824615 regulatory region variant T/G snp 0.26 0.700 1 2017 2017
dbSNP: rs1042133
rs1042133
2 6 33080829 stop lost G/C snp 0.14 0.15 0.700 1 2017 2017
dbSNP: rs10489481
rs10489481
2 1 185422035 intergenic variant G/A snp 0.30 0.700 1 2017 2017
dbSNP: rs10489673
rs10489673
2 1 157580276 intron variant T/C,G snp 0.43; 8.0E-06 0.35 0.700 1 2011 2011
dbSNP: rs10489844
rs10489844
2 1 158758599 intron variant C/T snp 0.25 0.700 1 2011 2011