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: rs104894220
rs104894220
DRD2
1 1.000 0.040 11 113416935 missense variant C/T snv 4.4E-05 6.3E-05 0.010 1.000 1 2000 2000
dbSNP: rs184841813
rs184841813
CACNA1B
1 1.000 0.040 9 138058108 missense variant G/A snv 4.3E-04 4.2E-04 0.010 < 0.001 1 2015 2015
dbSNP: rs746331571
rs746331571
SGCE ; CASD1
1 1.000 0.040 7 94618836 missense variant C/A;T snv 4.4E-05 0.010 1.000 1 2015 2015
dbSNP: rs786205860
rs786205860
KCTD17
2 0.925 0.040 22 37057420 missense variant G/A snv 0.010 1.000 1 2015 2015