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: rs10183640
rs10183640
2 2 157923692 intron variant G/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs10765792
rs10765792
2 11 96133536 intron variant G/C snv 0.10 0.700 1.000 1 2011 2011
dbSNP: rs10829156
rs10829156
2 10 18661626 intron variant T/C snv 0.79 0.700 1.000 1 2011 2011
dbSNP: rs10833905
rs10833905
2 11 23023046 regulatory region variant T/A snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs11187837
rs11187837
2 10 94276223 intron variant T/C snv 8.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs11624056
rs11624056
2 14 87039904 intergenic variant A/T snv 8.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs12155623
rs12155623
2 8 48899642 regulatory region variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12189362
rs12189362
2 5 153677988 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs12429889
rs12429889
2 13 74168185 intergenic variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs13022357
rs13022357
2 2 159213245 intron variant A/G snv 0.83 0.700 1.000 1 2011 2011
dbSNP: rs1554218
rs1554218
1 2 232894174 intron variant G/T snv 8.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs1559040
rs1559040
2 2 54120613 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs16866933
rs16866933
2 2 179701951 intron variant G/A snv 9.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs16872085
rs16872085
2 8 104945312 intron variant A/G snv 7.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs16942421
rs16942421
2 18 26576461 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17291650
rs17291650
2 12 50819650 synonymous variant A/G snv 6.7E-02 6.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs17718586
rs17718586
2 17 70648048 intergenic variant G/T snv 7.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs1823172
rs1823172
2 12 127308069 intergenic variant C/T snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs2077316
rs2077316
1 10 62465689 intron variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2251393
rs2251393
3 1.000 0.080 17 62701571 3 prime UTR variant G/A;C snv 0.85; 4.9E-05 0.700 1.000 1 2011 2011
dbSNP: rs2281680
rs2281680
2 14 23563861 splice region variant C/T snv 0.18 0.13 0.700 1.000 1 2011 2011
dbSNP: rs2389202
rs2389202
2 4 116333133 intergenic variant A/T snv 0.78 0.700 1.000 1 2011 2011
dbSNP: rs2824292
rs2824292
3 0.925 0.080 21 17414857 regulatory region variant G/A snv 0.47 0.700 1.000 1 2011 2011
dbSNP: rs2982694
rs2982694
2 6 151964552 intron variant G/T snv 0.86 0.700 1.000 1 2011 2011
dbSNP: rs4621553
rs4621553
2 5 113694467 intergenic variant G/A snv 0.78 0.700 1.000 1 2011 2011