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: rs10858583
rs10858583
LOC107984478
3 1.000 0.040 12 87334666 intergenic variant C/T snv 0.79 0.700 1.000 1 2016 2016
dbSNP: rs12149074
rs12149074
LOC105371357
3 1.000 0.040 16 80071969 intron variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs12475512
rs12475512 		2 2 231433365 downstream gene variant G/A snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs13077017
rs13077017
FLNB
2 3 58120049 intron variant C/T snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs13086738
rs13086738
SOX2-OT
3 1.000 0.040 3 181080939 intron variant A/G snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs138206701
rs138206701
RASGRF2
2 5 81110747 intron variant A/G snv 1.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs1805576
rs1805576
FXR1
3 1.000 0.040 3 180949777 intron variant C/G;T snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs4148087
rs4148087
ABCG1
3 1.000 0.040 21 42202157 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs4854912
rs4854912
SOX2-OT
3 1.000 0.040 3 181063312 intron variant C/T snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs7322916
rs7322916
ATP8A2
2 13 25433839 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs74566133
rs74566133 		2 8 133766099 regulatory region variant C/T snv 2.6E-02 0.700 1.000 1 2013 2013