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: rs494560
rs494560
1 1.000 0.040 11 118650844 non coding transcript exon variant A/G snv 0.57 0.710 1.000 2 2011 2012
dbSNP: rs10842893
rs10842893
1 1.000 0.040 12 27269953 intron variant C/T snv 7.1E-02 0.710 1.000 1 2019 2019
dbSNP: rs4774756
rs4774756
1 1.000 0.040 15 55254859 intron variant A/C snv 0.66 0.710 1.000 1 2019 2019
dbSNP: rs10069690
rs10069690
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 3 2015 2018
dbSNP: rs12803321
rs12803321
2 1.000 0.040 11 118609400 intron variant G/C;T snv 0.700 1.000 3 2015 2018
dbSNP: rs75061358
rs75061358
4 0.882 0.040 7 54848587 intergenic variant T/C;G snv 0.700 1.000 3 2015 2018
dbSNP: rs10464870
rs10464870
3 0.882 0.040 8 129465577 intron variant C/T snv 0.80 0.700 1.000 2 2009 2011
dbSNP: rs12752552
rs12752552
4 0.882 0.040 1 64763616 intron variant T/C snv 0.13 0.700 1.000 2 2017 2018
dbSNP: rs16904140
rs16904140
1 1.000 0.040 8 129653397 intron variant G/A snv 0.19 0.700 1.000 2 2009 2011
dbSNP: rs648044
rs648044
4 0.882 0.040 11 114160077 non coding transcript exon variant A/G;T snv 0.700 1.000 2 2015 2017
dbSNP: rs10116277
rs10116277
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs10120688
rs10120688
7 0.807 0.080 9 22056500 intron variant G/A snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs10131032
rs10131032
2 1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs10494090
rs10494090
2 1.000 0.040 1 108150714 intron variant A/C;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10852606
rs10852606
4 0.882 0.040 16 50094961 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10892258
rs10892258
4 0.925 0.120 11 118709156 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs10924303
rs10924303
2 1.000 0.040 1 245683732 intron variant C/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs10924690
rs10924690
2 1.000 0.040 1 246320481 intron variant G/A snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs11163687
rs11163687
2 1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs11166389
rs11166389
2 1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs111696067
rs111696067
2 1.000 0.040 12 132799954 intron variant T/C snv 5.3E-04 0.700 1.000 1 2015 2015
dbSNP: rs11216930
rs11216930
2 1.000 0.040 11 118618067 intron variant A/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs11216943
rs11216943
1 1.000 0.040 11 118685689 downstream gene variant G/A snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs11233250
rs11233250
4 0.882 0.040 11 82685972 intron variant C/T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs11583706
rs11583706
2 1.000 0.040 1 238358337 intron variant G/T snv 0.17 0.700 1.000 1 2009 2009