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: 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: rs10045431
rs10045431 		4 0.851 0.240 5 159387525 intron variant A/C snv 0.78 0.700 1.000 1 2011 2011
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: rs10142119
rs10142119 		1 1.000 0.080 14 98020208 intergenic variant G/A;C snv 0.700 1.000 1 2013 2013
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: 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: 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: rs10211025
rs10211025 		1 1.000 0.080 2 41801493 intergenic variant A/G snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs10268774
rs10268774 		1 1.000 0.080 7 82453122 intergenic variant T/C snv 3.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs10411428
rs10411428 		1 1.000 0.080 19 52104512 intergenic variant C/T snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs10413947
rs10413947 		1 1.000 0.080 19 9017666 upstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10414065
rs10414065 		4 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs10485681
rs10485681 		1 1.000 0.080 20 41864432 intergenic variant A/G snv 8.8E-02 0.700 1.000 1 2015 2015
dbSNP: rs10508372
rs10508372 		1 1.000 0.080 10 8930055 intergenic variant G/A snv 0.14 0.800 1.000 1 2011 2011
dbSNP: rs10515922
rs10515922 		1 1.000 0.080 2 102298194 regulatory region variant A/G snv 6.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs10667251
rs10667251 		4 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 0.700 1.000 1 2019 2019
dbSNP: rs10758669
rs10758669 		10 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10759931
rs10759931 		9 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs10769691
rs10769691 		1 1.000 0.080 11 6354579 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10795656
rs10795656 		4 1.000 0.080 10 8553876 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10795672
rs10795672 		2 0.925 0.080 10 8735677 intergenic variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10800812
rs10800812 		1 1.000 0.080 1 202086810 intergenic variant A/G snv 0.77 0.700 1.000 1 2000 2000
dbSNP: rs10811516
rs10811516 		1 1.000 0.080 9 21255050 intergenic variant C/A;T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs10924993
rs10924993 		2 0.925 0.080 1 236296485 intergenic variant T/A;G snv 0.010 1.000 1 2008 2008