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: rs10801153
rs10801153 		3 0.925 0.080 1 192794818 intron variant G/A snv 0.27 0.010 1.000 1 2015 2015
dbSNP: rs11059336
rs11059336 		1 12 127745489 regulatory region variant T/C snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs113209956
rs113209956 		1 9 25211195 intergenic variant C/T snv 5.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs1192553
rs1192553 		1 1 17967858 intergenic variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs1458103
rs1458103 		1 11 81336231 intron variant A/C snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs2463107
rs2463107 		2 1.000 0.040 12 79699537 intron variant A/C snv 0.36 0.010 1.000 1 2010 2010
dbSNP: rs2572431
rs2572431 		2 1.000 0.040 8 11247568 downstream gene variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs34548976
rs34548976 		2 1.000 0.040 7 31032854 intergenic variant C/T snv 0.39 0.010 1.000 1 2015 2015
dbSNP: rs4813627
rs4813627 		2 1.000 0.040 20 3074867 downstream gene variant A/G snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs72711240
rs72711240 		1 4 134774652 intron variant C/T snv 2.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs7766029
rs7766029 		7 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs9875578
rs9875578 		1 3 13752941 intergenic variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs1202184
rs1202184
ABCB1
7 0.851 0.120 7 87584585 intron variant C/T snv 0.39 0.010 1.000 1 2011 2011
dbSNP: rs1922242
rs1922242
ABCB1
8 0.827 0.120 7 87544351 intron variant A/T snv 0.43 0.010 1.000 1 2011 2011
dbSNP: rs1401663578
rs1401663578
ACE
4 0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 0.010 1.000 1 2017 2017
dbSNP: rs2451828
rs2451828
ADCY2
1 5 7448683 intron variant C/T snv 2.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs4822492
rs4822492
ADORA2A-AS1
4 1.000 0.040 22 24447626 intron variant C/G snv 0.47 0.010 1.000 1 2008 2008
dbSNP: rs5751876
rs5751876
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
16 0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 0.050 1.000 5 2008 2016
dbSNP: rs2298383
rs2298383
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
11 0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 0.020 1.000 2 2008 2019
dbSNP: rs3761422
rs3761422
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
4 1.000 0.040 22 24430704 intron variant T/C snv 0.62 0.010 < 0.001 1 2010 2010
dbSNP: rs3930965
rs3930965
AKR1C1
2 1.000 0.040 10 4971951 intron variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs900418273
rs900418273
ANKK1
8 0.807 0.120 11 113393764 missense variant A/G snv 0.010 1.000 1 2008 2008
dbSNP: rs63750264
rs63750264
APP
17 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2004 2004
dbSNP: rs63750579
rs63750579
APP
13 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs2306073
rs2306073
ARNTL2 ; ARNTL2-AS1
4 0.882 0.080 12 27402904 intron variant C/T snv 0.37 0.010 1.000 1 2012 2012