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: rs505922
rs505922
ABO
34 0.689 0.520 9 133273813 intron variant C/T snv 0.810 1.000 1 2012 2012
dbSNP: rs657152
rs657152
ABO
22 0.882 0.200 9 133263862 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7046863
rs7046863 		1 1.000 0.040 9 133246054 downstream gene variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs7855466
rs7855466 		3 0.925 0.080 9 133245916 downstream gene variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs9411471
rs9411471 		2 1.000 0.040 9 133244704 intergenic variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs9919007
rs9919007 		2 1.000 0.040 9 133244140 intergenic variant C/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1800470
rs1800470
TGFB1
107 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007
dbSNP: rs1800471
rs1800471
TGFB1
48 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2007 2007