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: rs1106683
rs1106683 		3 7 131768766 intergenic variant G/A snv 0.14 0.700 1.000 1 2007 2007
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs16986921
rs16986921
CTNNBL1
3 1.000 0.080 20 37754119 intron variant C/T snv 0.12 0.700 1.000 1 2008 2008
dbSNP: rs6013029
rs6013029
CTNNBL1
5 0.882 0.160 20 37771178 intron variant G/T snv 0.12 0.700 1.000 1 2008 2008
dbSNP: rs6020712
rs6020712
CTNNBL1
4 1.000 0.080 20 37758210 intron variant G/A snv 0.12 0.700 1.000 1 2008 2008
dbSNP: rs7001819
rs7001819
LOC105379243
4 0.925 0.080 8 11792966 upstream gene variant T/C snv 0.35 0.700 1.000 1 2008 2008
dbSNP: rs7498665
rs7498665
SH2B1
9 0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 0.700 1.000 2 2009 2009
dbSNP: rs7561317
rs7561317 		7 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 0.700 1.000 2 2009 2009
dbSNP: rs10173167
rs10173167 		2 2 646767 intergenic variant G/A snv 0.82 0.700 1.000 1 2009 2009
dbSNP: rs10188334
rs10188334 		2 2 653874 regulatory region variant C/A;T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs10193244
rs10193244 		2 2 647580 intergenic variant T/C snv 0.77 0.700 1.000 1 2009 2009
dbSNP: rs10769908
rs10769908
STK33
4 11 8462542 intron variant C/T snv 0.55 0.700 1.000 1 2009 2009
dbSNP: rs10838738
rs10838738
MTCH2
6 1.000 0.080 11 47641497 intron variant A/G snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs10913469
rs10913469
SEC16B ; CRYZL2P-SEC16B
7 1.000 0.080 1 177944384 intron variant T/C snv 0.22 0.700 1.000 1 2009 2009
dbSNP: rs11084753
rs11084753 		6 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 0.700 1.000 1 2009 2009
dbSNP: rs12714414
rs12714414 		2 2 651407 intergenic variant T/C snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs12714415
rs12714415 		4 2 651430 intergenic variant T/C snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs1320336
rs1320336 		2 2 650012 intergenic variant G/A snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs1320337
rs1320337 		2 2 649867 intergenic variant A/T snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs1320338
rs1320338 		2 2 649347 intergenic variant T/G snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs13386517
rs13386517 		2 2 650479 regulatory region variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs13386627
rs13386627 		2 2 650560 regulatory region variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13386964
rs13386964 		2 2 650828 regulatory region variant G/A snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs13388043
rs13388043 		2 2 637597 regulatory region variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13393304
rs13393304 		2 2 637830 regulatory region variant A/C;G snv 0.700 1.000 1 2009 2009