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: rs11110077
rs11110077
ANKS1B
1 12 99872335 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11214606
rs11214606
DRD2
1 11 113439147 intron variant C/T snv 3.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs114144395
rs114144395
DNAH12
1 3 57409292 intron variant C/T snv 7.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs11677416
rs11677416 		2 1.000 0.040 2 112771663 downstream gene variant T/C snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs12726652
rs12726652 		1 1 106889954 intergenic variant G/A snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs148396385
rs148396385
LINC01818
1 2 150317207 intron variant C/G snv 9.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs17396139
rs17396139 		1 4 161364214 intergenic variant G/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs17511050
rs17511050 		1 4 132921496 intron variant C/T snv 2.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs35751312
rs35751312 		1 5 174792997 intron variant T/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs474357
rs474357 		1 11 82726076 downstream gene variant G/A snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs4805924
rs4805924
CHST8
1 19 33677367 intron variant C/T snv 3.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs62288757
rs62288757 		1 3 192077447 downstream gene variant T/G snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs6856328
rs6856328
ADGRL3
1 4 61571600 intron variant C/G snv 6.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs73481300
rs73481300
MS4A5
1 11 60450348 intron variant C/T snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs75024542
rs75024542
SH3GL3
1 15 83523366 intron variant G/C snv 2.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs7520258
rs7520258
GPR137B
1 1 236149827 intron variant T/C snv 7.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs7566497
rs7566497
FRZB
1 2 182859894 intron variant A/G snv 3.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs7770731
rs7770731
LOC101928354
1 6 14598589 intron variant T/C snv 0.28 0.700 1.000 1 2011 2011