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: rs1321311
rs1321311 		15 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 0.700 1.000 2 2010 2016
dbSNP: rs10850409
rs10850409 		2 12 114943935 intergenic variant G/A snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs11153730
rs11153730 		4 6 118346359 intergenic variant T/C snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs12036340
rs12036340 		2 1 162045950 intergenic variant A/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs12039739
rs12039739 		1 1 115790490 regulatory region variant C/T snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs13165478
rs13165478 		3 5 154489480 upstream gene variant G/A snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs13185595
rs13185595 		1 5 154492610 upstream gene variant G/A snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs1344852
rs1344852 		1 4 20182314 intergenic variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1362212
rs1362212 		2 7 35265695 intergenic variant G/A snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs1419856
rs1419856 		1 7 35267372 intergenic variant A/G snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs17391905
rs17391905 		2 1 51080468 intergenic variant T/G snv 3.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs4708832
rs4708832 		1 6 159472905 intron variant G/T snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs6968945
rs6968945 		1 7 46601302 intergenic variant C/T snv 0.61 0.700 1.000 1 2016 2016
dbSNP: rs7132327
rs7132327 		1 12 114943266 intergenic variant T/C snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs7771320
rs7771320 		1 6 7502516 upstream gene variant T/C snv 5.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs7784776
rs7784776 		2 7 46580547 intergenic variant A/G snv 0.42 0.700 1.000 1 2016 2016
dbSNP: rs9470361
rs9470361 		12 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs9851724
rs9851724 		2 3 38678444 intergenic variant C/T snv 0.73 0.700 1.000 1 2016 2016
dbSNP: rs1562782
rs1562782
AMPD3 ; CAND1.11
1 11 10321164 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs7909027
rs7909027
CACNB2
1 10 18406963 intron variant T/C snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs4642101
rs4642101
CAND2
3 1.000 0.080 3 12800724 intron variant T/G snv 0.63 0.700 1.000 1 2016 2016
dbSNP: rs3929778
rs3929778
CASC20
1 20 6479643 intron variant C/T snv 0.84 0.700 1.000 1 2016 2016
dbSNP: rs4074536
rs4074536
CASQ2
2 1 115768346 missense variant T/C snv 0.33 0.34 0.700 1.000 1 2016 2016
dbSNP: rs7537765
rs7537765
CLCN6
1 1 11827246 intron variant A/G snv 0.15 0.18 0.700 1.000 1 2016 2016
dbSNP: rs359466
rs359466
CPEB4
1 5 173888863 5 prime UTR variant C/G snv 0.11 0.700 1.000 1 2016 2016