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: rs2345039
rs2345039
ADGRL3
2 0.925 0.040 4 61899312 intron variant G/C snv 0.42 0.010 1.000 1 2019 2019
dbSNP: rs6280
rs6280
DRD3
57 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 0.010 1.000 1 2002 2002
dbSNP: rs6295
rs6295
HTR1A
40 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2010 2010
dbSNP: rs9525584
rs9525584
DGKH
2 0.925 0.040 13 42160758 intron variant T/C snv 0.46 0.010 1.000 1 2019 2019
dbSNP: rs9566845
rs9566845
VWA8
3 0.925 0.040 13 41761944 intron variant G/A snv 6.1E-02 0.010 1.000 1 2010 2010
dbSNP: rs994856
rs994856
DGKH
2 0.925 0.040 13 42134315 intron variant A/G snv 0.37 0.010 1.000 1 2019 2019