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: rs10428959
rs10428959
DOCK4
1 7 112037851 intron variant C/T snv 3.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs10952132
rs10952132 		1 7 9027190 intergenic variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11574703
rs11574703
CD36
1 7 80657592 intron variant T/C snv 1.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs11766298
rs11766298
AHCYL2
1 7 129365006 intron variant C/T snv 3.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs9285640
rs9285640
PPARGC1B
1 5 149762504 intron variant G/A;C snv 0.700 1.000 1 2012 2012