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: rs1007392
rs1007392
PDE3B
2 11 14753045 intron variant A/G snv 0.35 0.700 1.000 1 2014 2014
dbSNP: rs10485165
rs10485165
LOC105377885
3 6 88403098 intron variant C/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs10745742
rs10745742
AMDHD1
2 12 95964751 intron variant C/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs11023332
rs11023332
PDE3B
2 11 14762564 intron variant G/C snv 0.35 0.700 1.000 1 2014 2014
dbSNP: rs11586313
rs11586313 		2 1 152917994 TF binding site variant G/A;C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs116970203
rs116970203
PDE3B
2 11 14855172 intron variant G/A snv 2.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs117300835
rs117300835 		2 11 15097429 intergenic variant G/A snv 7.6E-03 0.700 1.000 1 2017 2017
dbSNP: rs117865811
rs117865811
SPON1
2 11 14180763 intron variant A/G snv 6.3E-03 0.700 1.000 1 2017 2017
dbSNP: rs117913124
rs117913124
CYP2R1
2 11 14879385 synonymous variant G/A snv 1.7E-02 1.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs12287212
rs12287212 		2 11 14428315 intergenic variant C/A snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs12868495
rs12868495 		2 13 34067425 intergenic variant G/A snv 2.3E-02 0.700 1.000 1 2014 2014
dbSNP: rs13107347
rs13107347
NPFFR2
2 4 72109031 intron variant T/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs138485827
rs138485827 		2 4 72166226 intergenic variant C/T snv 5.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs1410656
rs1410656 		2 13 46968386 intergenic variant T/C snv 0.97 0.700 1.000 1 2018 2018
dbSNP: rs148189294
rs148189294 		2 4 71575200 downstream gene variant G/A snv 2.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs1526692
rs1526692 		2 4 71713007 intergenic variant A/G snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs156299
rs156299
LOC107986777
2 7 24185113 intergenic variant T/G snv 0.53 0.700 1.000 1 2014 2014
dbSNP: rs1607741
rs1607741 		2 4 71853316 intergenic variant G/C snv 0.65 0.700 1.000 1 2017 2017
dbSNP: rs17216707
rs17216707 		6 20 54115823 intergenic variant T/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs17767445
rs17767445 		2 4 71879550 intergenic variant G/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs182244780
rs182244780
RRAS2
2 11 14363985 intron variant G/A snv 6.0E-03 0.700 1.000 1 2017 2017
dbSNP: rs185378533
rs185378533
FLJ42102
2 11 71422087 intron variant A/G snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs2207173
rs2207173
LOC105372568
2 20 22824423 intergenic variant G/A snv 0.72 0.700 1.000 1 2016 2016
dbSNP: rs2277458
rs2277458
GEMIN2 ; LOC105370459
2 14 39114277 5 prime UTR variant A/G snv 0.80 0.83 0.700 1.000 1 2017 2017
dbSNP: rs2302190
rs2302190
MTMR4
3 17 58507147 missense variant T/A;C snv 0.24 0.700 1.000 1 2014 2014