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: rs548097
rs548097 		1 1.000 0.040 13 75202132 intergenic variant G/C;T snv 0.800 1.000 1 2010 2010
dbSNP: rs562338
rs562338 		21 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 0.700 1.000 1 2016 2016
dbSNP: rs61945053
rs61945053 		3 1.000 0.040 13 27021678 upstream gene variant G/A snv 2.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs6533530
rs6533530 		16 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 0.700 1.000 1 2016 2016
dbSNP: rs74056623
rs74056623 		3 1.000 0.040 1 18784584 intergenic variant G/A snv 8.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs74056624
rs74056624 		3 1.000 0.040 1 18790006 intergenic variant G/A snv 2.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs765547
rs765547 		18 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7703051
rs7703051 		18 0.851 0.120 5 75329662 intron variant C/A snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs79661299
rs79661299 		3 1.000 0.040 6 42088268 downstream gene variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs799165
rs799165 		17 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs8082812
rs8082812 		16 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs9351814
rs9351814 		4 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs9885413
rs9885413 		2 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 0.710 1.000 1 2016 2016
dbSNP: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 1999 1999
dbSNP: rs1799752
rs1799752
ACE
25 0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 0.010 1.000 1 2014 2014
dbSNP: rs2210327
rs2210327
ADAMTSL1
1 1.000 0.040 9 18109237 intron variant A/T snv 3.4E-02 0.800 1.000 1 2010 2010
dbSNP: rs1801253
rs1801253
ADRB1
34 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.100 0.917 12 2003 2019
dbSNP: rs1801252
rs1801252
ADRB1
17 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 0.060 1.000 6 2000 2019
dbSNP: rs1042713
rs1042713
ADRB2
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.040 1.000 4 2007 2018
dbSNP: rs1042714
rs1042714
ADRB2
54 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 0.020 0.500 2 2010 2018
dbSNP: rs1800888
rs1800888
ADRB2
23 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.020 1.000 2 2009 2010
dbSNP: rs1800624
rs1800624
AGER ; PBX2
33 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs1800625
rs1800625
AGER ; PBX2
39 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 0.010 1.000 1 2012 2012
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.040 1.000 4 1999 2014
dbSNP: rs4762
rs4762
AGT
35 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 2007 2007