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: rs1158867
rs1158867
3 1.000 0.080 2 127419801 splice region variant C/T snv 0.51 0.800 1.000 1 2010 2010
dbSNP: rs17145713
rs17145713
6 0.925 0.120 7 73490480 intron variant C/T snv 0.21 0.800 1.000 1 2010 2010
dbSNP: rs6120849
rs6120849
2 20 35142584 intron variant C/T snv 0.19 0.800 1.000 1 2010 2010
dbSNP: rs1011019
rs1011019
2 2 127279984 intron variant A/G;T snv 0.75 0.700 1.000 1 2010 2010
dbSNP: rs1018503
rs1018503
2 20 34737712 intron variant T/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs1019842
rs1019842
2 2 127547621 intron variant T/C snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs10208529
rs10208529
5 0.925 0.120 2 27563321 intron variant A/T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs1033797
rs1033797
2 20 35131884 intron variant T/C snv 0.27 0.700 1.000 1 2010 2010
dbSNP: rs1033799
rs1033799
2 20 35132230 intron variant C/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs1040552
rs1040552
2 20 33861523 regulatory region variant A/G snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs10485505
rs10485505
3 1.000 0.080 20 34437762 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs10485508
rs10485508
2 20 35017295 intron variant C/T snv 8.0E-02 0.700 1.000 1 2010 2010
dbSNP: rs10496661
rs10496661
2 2 127332568 intron variant G/T snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs1058003
rs1058003
2 20 35002614 3 prime UTR variant G/A snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs10803588
rs10803588
2 2 127570800 intron variant C/T snv 0.37 0.700 1.000 1 2010 2010
dbSNP: rs10875492
rs10875492
2 20 35043604 intron variant C/T snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs10928772
rs10928772
2 2 127584028 intron variant T/G snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs11167260
rs11167260
2 20 35187397 intron variant G/A snv 9.1E-02 0.700 1.000 1 2010 2010
dbSNP: rs1124511
rs1124511
2 20 35148894 upstream gene variant A/C snv 0.48 0.700 1.000 1 2010 2010
dbSNP: rs1160297
rs1160297
3 2 53010182 intergenic variant G/C snv 0.69 0.700 1.000 1 2007 2007
dbSNP: rs11679414
rs11679414
2 2 127393427 intron variant G/A snv 0.27 0.700 1.000 1 2010 2010
dbSNP: rs11680949
rs11680949
2 2 127365986 intron variant C/G snv 0.25 0.700 1.000 1 2010 2010
dbSNP: rs11683427
rs11683427
2 2 127198967 intron variant A/G snv 0.22 0.700 1.000 1 2010 2010
dbSNP: rs11683986
rs11683986
2 2 127438822 intron variant C/T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs11691088
rs11691088
2 2 127374277 non coding transcript exon variant A/G snv 0.27 0.700 1.000 1 2010 2010