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: rs10138032
rs10138032
HIF1A ; HIF1A-AS3
1 14 61717464 intron variant A/G snv 8.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs10152811
rs10152811
AGBL1 ; AGBL1-AS1
1 15 86311359 intron variant A/C snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs10199914
rs10199914 		1 2 238975165 regulatory region variant A/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs10281741
rs10281741
PTPRN2
1 7 158000430 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10305923
rs10305923
EDNRA
1 4 147539622 intron variant T/C snv 2.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10417097
rs10417097
PBX4
1 19 19609015 intron variant C/G snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs10419349
rs10419349
VAV1
1 19 6836678 intron variant C/T snv 2.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs10438303
rs10438303 		1 15 43724219 downstream gene variant T/C snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs10459452
rs10459452
ESR2
1 14 64245143 intron variant A/G snv 4.4E-03 0.700 1.000 1 2012 2012
dbSNP: rs10466588
rs10466588 		1 11 116739533 regulatory region variant A/G snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs10474433
rs10474433 		1 5 75321018 intron variant T/C snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs10475588
rs10475588 		1 5 173227744 upstream gene variant T/C snv 2.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10495712
rs10495712 		1 2 20973240 intergenic variant A/G snv 0.77 0.700 1.000 1 2009 2009
dbSNP: rs1051795
rs1051795
POLK
1 5 75600973 3 prime UTR variant G/A snv 0.22 0.700 1.000 1 2009 2009
dbSNP: rs10518983
rs10518983
LIPC
1 15 58520578 intron variant C/T snv 5.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs10519948
rs10519948
NR3C2
1 4 148230877 intron variant C/G snv 1.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs1065314
rs1065314
TIMP3 ; SYN3
1 22 32862301 3 prime UTR variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1078424
rs1078424
UBE3B
1 12 109532300 intron variant G/A snv 9.1E-03 0.700 1.000 1 2012 2012
dbSNP: rs10790495
rs10790495
MIR100HG
1 11 122327998 intron variant A/G snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs10793310
rs10793310
GAB2
1 11 78387968 intron variant T/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs1079596
rs1079596
DRD2
1 11 113425897 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10838852
rs10838852
OR4X1
1 11 48264704 missense variant C/T snv 0.52 0.46 0.700 1.000 1 2009 2009
dbSNP: rs10853981
rs10853981 		1 19 4965053 upstream gene variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10873925
rs10873925
ST6GALNAC5
1 1 76996050 intron variant A/G snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs10919021
rs10919021
NOS1AP
1 1 162265600 intron variant C/T snv 0.97 0.700 1.000 1 2012 2012