Source: ALL
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: rs10131567
rs10131567
1 1.000 0.040 14 35395672 intergenic variant G/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs10244416
rs10244416
1 1.000 0.040 7 20536128 intergenic variant C/A;T snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs1025549
rs1025549
1 1.000 0.040 2 198016459 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1032841
rs1032841
1 1.000 0.040 2 8526108 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10468514
rs10468514
1 1.000 0.040 17 45378874 intergenic variant A/G snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs10489854
rs10489854
1 1.000 0.040 1 159279069 non coding transcript exon variant C/T snv 8.3E-02 0.010 1.000 1 2010 2010
dbSNP: rs10756796
rs10756796
1 1.000 0.040 9 16730976 intron variant A/G snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs10822037
rs10822037
1 1.000 0.040 10 62616798 intron variant T/C snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs10910095
rs10910095
2 1.000 0.040 1 2579316 upstream gene variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10937319
rs10937319
1 1.000 0.040 3 187711669 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10947428
rs10947428
2 1.000 0.040 6 33679281 intron variant T/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs10991797
rs10991797
1 1.000 0.040 9 91168389 intron variant A/G snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs111267073
rs111267073
1 1.000 0.040 5 111030094 intergenic variant C/T snv 1.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs11213941
rs11213941
1 1.000 0.040 11 111563369 downstream gene variant T/C snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs11242709
rs11242709
2 1.000 0.040 6 209159 upstream gene variant C/T snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs11255753
rs11255753
2 1.000 0.040 10 8563590 intergenic variant G/C;T snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs11265449
rs11265449
1 1.000 0.040 1 160612458 intron variant C/G snv 0.45 0.36 0.700 1.000 1 2019 2019
dbSNP: rs114269697
rs114269697
3 1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs11466681
rs11466681
1 1.000 0.040 1 1206007 intron variant C/T snv 6.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs114997373
rs114997373
1 1.000 0.040 1 45535906 downstream gene variant G/A snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs115390301
rs115390301
1 1.000 0.040 1 149981477 intron variant G/A snv 1.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs11539209
rs11539209
2 1.000 0.040 9 128721272 missense variant T/A;C snv 7.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs11626205
rs11626205
1 1.000 0.040 14 92558117 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs11736191
rs11736191
1 1.000 0.040 4 4766748 intron variant T/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs11783015
rs11783015
1 1.000 0.040 8 128682763 intron variant T/C snv 0.23 0.700 1.000 1 2019 2019