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: rs1508147
rs1508147 		1 1.000 0.080 17 78226507 upstream gene variant G/A snv 0.38 0.010 1.000 1 2012 2012
dbSNP: rs1800810
rs1800810
PDGFRA
1 1.000 0.080 4 54227864 intron variant C/A;G snv 0.010 1.000 1 2006 2006
dbSNP: rs1805014
rs1805014
IL4R
4 0.851 0.080 16 27363708 missense variant T/C snv 7.4E-03 1.4E-02 0.010 1.000 1 2001 2001
dbSNP: rs2579931
rs2579931
GRIK2
1 1.000 0.080 6 101406757 intron variant G/A;C;T snv 0.010 1.000 1 2014 2014
dbSNP: rs9851461
rs9851461
LOC105374041
1 1.000 0.080 3 112392234 downstream gene variant T/C snv 4.9E-02 0.010 1.000 1 2014 2014