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: rs10008032
rs10008032
2 1.000 0.080 4 38743861 intergenic variant T/C snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs10021288
rs10021288
1 1.000 0.080 4 122084379 downstream gene variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs10036748
rs10036748
11 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2012 2012
dbSNP: rs10044254
rs10044254
2 0.925 0.080 5 15783487 intron variant A/G snv 0.25 0.700 1.000 1 2014 2014
dbSNP: rs10045431
rs10045431
4 0.851 0.240 5 159387525 intron variant A/C snv 0.78 0.700 1.000 1 2011 2011
dbSNP: rs10048897
rs10048897
1 1.000 0.080 22 17777938 non coding transcript exon variant T/C snv 9.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs10056243
rs10056243
1 1.000 0.080 5 110923378 intergenic variant G/A snv 8.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs10056340
rs10056340
3 0.925 0.080 5 110854353 intergenic variant T/G snv 0.31 0.010 1.000 1 2017 2017
dbSNP: rs10074523
rs10074523
2 1.000 0.080 5 132724891 intron variant C/A snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs1007654
rs1007654
1 1.000 0.080 17 39955101 intron variant A/G snv 0.69 0.700 1.000 1 2010 2010
dbSNP: rs1008723
rs1008723
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.800 1.000 2 2011 2019
dbSNP: rs1012307
rs1012307
1 1.000 0.080 2 149798707 intron variant A/C snv 4.9E-02 0.700 1.000 1 2014 2014
dbSNP: rs10131490
rs10131490
1 1.000 0.080 14 68276590 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10142119
rs10142119
1 1.000 0.080 14 98020208 intergenic variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10152595
rs10152595
2 1.000 0.080 15 67183150 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10158467
rs10158467
2 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10173081
rs10173081
2 1.000 0.080 2 102340888 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs1017494
rs1017494
2 1.000 0.080 2 234770601 regulatory region variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10174949
rs10174949
2 1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs10178845
rs10178845
2 1.000 0.080 2 8303673 intron variant G/A snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs10187276
rs10187276
2 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 0.700 1.000 2 2019 2019
dbSNP: rs10189629
rs10189629
2 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs10192157
rs10192157
2 1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 0.710 1.000 2 2010 2020
dbSNP: rs10197862
rs10197862
3 0.925 0.120 2 102350089 intron variant A/G snv 0.18 0.810 1.000 3 2011 2014
dbSNP: rs10204137
rs10204137
2 0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 0.700 1.000 1 2010 2010