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: rs2306073
rs2306073
ARNTL2 ; ARNTL2-AS1
4 0.882 0.080 12 27402904 intron variant C/T snv 0.37 0.020 1.000 2 2010 2012
dbSNP: rs25531
rs25531
SLC6A4 ; LOC105371720
72 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 0.010 1.000 1 2009 2009
dbSNP: rs4606
rs4606
RGS2
16 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs4964057
rs4964057
ARNTL2
3 0.882 0.080 12 27363909 intron variant T/G snv 0.29 0.010 1.000 1 2012 2012
dbSNP: rs53576
rs53576
CAV3 ; OXTR
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs6855911
rs6855911
SLC2A9
7 0.851 0.200 4 9934286 intron variant A/G snv 0.33 0.010 1.000 1 2013 2013
dbSNP: rs7131056
rs7131056
DRD2
6 0.827 0.200 11 113459052 intron variant A/C snv 0.51 0.010 1.000 1 2010 2010
dbSNP: rs7958822
rs7958822
ARNTL2
6 0.807 0.200 12 27348173 intron variant G/A snv 0.43 0.010 1.000 1 2012 2012