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: rs10498345
rs10498345 		1 1.000 0.040 14 38551301 intergenic variant T/A snv 6.4E-02 0.810 1.000 1 2007 2007
dbSNP: rs1890131
rs1890131
RCSD1
1 1.000 0.040 1 167628236 non coding transcript exon variant C/T snv 0.29 0.700 1.000 1 2007 2007
dbSNP: rs9300039
rs9300039 		4 0.851 0.160 11 41893816 intergenic variant C/A snv 9.8E-02 0.700 1.000 1 2007 2007
dbSNP: rs1799983
rs1799983
NOS3
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 1.000 6 1998 2011
dbSNP: rs662
rs662
PON1
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.020 1.000 2 2002 2011
dbSNP: rs11544238
rs11544238
MARS1 ; ARHGAP9
1 1.000 0.040 12 57476372 missense variant A/C;G snv 0.50; 8.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs61688134
rs61688134
ABCC9
3 0.882 0.080 12 21864476 missense variant C/T snv 7.4E-03 7.5E-03 0.010 1.000 1 2013 2013
dbSNP: rs76863441
rs76863441
PLA2G7
25 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 0.010 1.000 1 2002 2002
dbSNP: rs770804393
rs770804393
DLK1
3 0.882 0.240 14 100734514 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2002 2002