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: rs11047102
rs11047102
SOX5
2 0.925 0.160 12 23793212 intron variant C/T snv 7.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs11117432
rs11117432 		4 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 0.010 1.000 1 2015 2015
dbSNP: rs11642873
rs11642873 		4 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 0.010 1.000 1 2011 2011
dbSNP: rs12540874
rs12540874
GRB10
3 0.882 0.280 7 50597225 intron variant A/C;G snv 0.010 1.000 1 2011 2011
dbSNP: rs1372072
rs1372072
PLCL2
4 0.851 0.200 3 16913767 intron variant G/A snv 0.35 0.010 1.000 1 2015 2015
dbSNP: rs7665090
rs7665090
MANBA
6 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.010 1.000 1 2015 2015