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: rs11765649
rs11765649
1 7 23439394 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs12543725
rs12543725
1 8 141237880 intron variant G/A snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs12823128
rs12823128
1 12 26719797 intron variant T/C snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs12906125
rs12906125
FES
1 15 90884382 intron variant G/A snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs12942207
rs12942207
1 17 47890928 downstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1351394
rs1351394
5 12 65958046 3 prime UTR variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1374204
rs1374204
1 2 46257066 non coding transcript exon variant C/T snv 0.66 0.700 1.000 1 2016 2016
dbSNP: rs139975827
rs139975827
1 12 21915227 intron variant G/A snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs144843919
rs144843919
1 17 30710321 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1819436
rs1819436
1 13 78006148 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs2150052
rs2150052
1 9 111182787 intron variant A/T snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs2324499
rs2324499
1 13 40087864 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs2421016
rs2421016
3 0.925 0.120 10 122407996 intron variant C/T snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs2473248
rs2473248
1 1 22210150 intergenic variant T/C snv 0.83 0.700 1.000 1 2016 2016
dbSNP: rs28510415
rs28510415
1 9 95482744 non coding transcript exon variant A/G snv 6.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs28530618
rs28530618
2 20 32687779 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs2854355
rs2854355
RB1
1 13 48308227 intron variant A/G snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs3753639
rs3753639
1 1 155013615 intron variant T/C snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs4330912
rs4330912
1 1 155999637 intron variant C/G snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs6016377
rs6016377
1 20 40544088 intergenic variant C/T snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs61154119
rs61154119
1 19 8677915 downstream gene variant T/A;G snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs61862780
rs61862780
2 1.000 0.080 10 92708886 downstream gene variant T/C snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs62240962
rs62240962
1 22 41863520 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs62466330
rs62466330
1 7 73642475 intergenic variant T/C snv 4.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs6537307
rs6537307
1 4 144680711 intron variant A/G snv 0.39 0.700 1.000 1 2016 2016