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: rs17113859
rs17113859
1 1.000 0.080 14 28325689 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs17123980
rs17123980
1 1.000 0.080 20 33001967 intron variant G/A;C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs172137
rs172137
2 0.925 0.120 5 167604857 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs17645516
rs17645516
1 1.000 0.080 17 5786465 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1873962
rs1873962
1 1.000 0.080 11 25794628 intergenic variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1936900
rs1936900
1 1.000 0.080 6 19630984 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs2063481
rs2063481
1 1.000 0.080 3 24101810 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs2177755
rs2177755
1 1.000 0.080 7 123087497 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2305795
rs2305795
2 0.925 0.080 19 10115376 intron variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs2474121
rs2474121
1 1.000 0.080 1 85332355 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2523405
rs2523405
1 1.000 0.080 6 29727528 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs2679120
rs2679120
1 1.000 0.080 15 65205058 intron variant C/A;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2682912
rs2682912
1 1.000 0.080 15 77582926 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs2834188
rs2834188
1 1.000 0.080 21 33316948 regulatory region variant A/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs3101942
rs3101942
3 0.882 0.200 6 32902280 intergenic variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs3130311
rs3130311
3 0.882 0.200 6 32249590 intergenic variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs3134926
rs3134926
3 0.882 0.200 6 32232370 intergenic variant C/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs370063
rs370063
1 1.000 0.080 16 77944164 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs3797299
rs3797299
1 1.000 0.080 5 146493802 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs3806156
rs3806156
5 0.827 0.280 6 32405921 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs41321151
rs41321151
1 1.000 0.080 5 159728502 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs41427946
rs41427946
1 1.000 0.080 1 119566637 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs4234848
rs4234848
1 1.000 0.080 4 79929651 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs4320890
rs4320890
1 1.000 0.080 10 96625050 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs455674
rs455674
3 0.882 0.120 6 39768626 regulatory region variant C/G;T snv 0.700 1.000 1 2009 2009