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: rs887829
rs887829
18 0.763 0.280 2 233759924 intron variant C/T snv 0.36 0.700 1.000 2 2013 2014
dbSNP: rs10178992
rs10178992
4 2 233749231 intron variant T/A snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs10179091
rs10179091
4 2 233749337 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs10929301
rs10929301
4 2 233755003 splice region variant C/G;T snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs10929302
rs10929302
4 2 233757136 intron variant G/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs11673726
rs11673726
4 2 233755414 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs11888459
rs11888459
4 2 233747994 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs11891311
rs11891311
4 2 233730664 intron variant G/A snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs13009407
rs13009407
1 2 233743701 non coding transcript exon variant C/A;G;T snv 4.0E-06; 0.22; 4.0E-06 0.700 1.000 1 2013 2013
dbSNP: rs17862875
rs17862875
4 2 233740656 intron variant G/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs17864701
rs17864701
3 2 233744071 intron variant C/T snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs1983023
rs1983023
3 2 233728376 intron variant T/C snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs2008595
rs2008595
3 2 233728546 intron variant C/T snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs2018985
rs2018985
3 2 233740214 intron variant A/G snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs3755319
rs3755319
8 0.925 0.120 2 233758936 intron variant A/C;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs3771341
rs3771341
3 2 233764593 intron variant G/A;T snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs3806596
rs3806596
3 2 233729061 intron variant T/C snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs3806597
rs3806597
3 2 233728923 intron variant A/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs4124874
rs4124874
8 0.851 0.120 2 233757013 intron variant T/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs4148324
rs4148324
4 2 233764076 intron variant T/A;G snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs4148325
rs4148325
11 0.851 0.080 2 233764663 intron variant C/T snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs4148326
rs4148326
5 0.925 0.080 2 233764816 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs4399719
rs4399719
3 2 233757815 intron variant T/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs4663333
rs4663333
3 2 233746657 intron variant G/T snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs4663963
rs4663963
3 2 233741547 non coding transcript exon variant T/G snv 0.55 0.700 1.000 1 2013 2013