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: rs7579899
rs7579899
2 0.925 0.120 2 46310465 intron variant A/G snv 0.52 0.830 1.000 5 2011 2019
dbSNP: rs11894252
rs11894252
3 0.925 0.120 2 46306237 intron variant T/A;C;G snv 0.810 1.000 4 2011 2019
dbSNP: rs2121266
rs2121266
1 1.000 0.120 2 46308785 intron variant C/A snv 0.61 0.800 1.000 2 2011 2019
dbSNP: rs10211665
rs10211665
1 1.000 0.120 2 46298957 intron variant T/C snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs11125068
rs11125068
1 1.000 0.120 2 46300677 intron variant A/G snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs11684885
rs11684885
1 1.000 0.120 2 46306413 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs11689011
rs11689011
2 1.000 0.120 2 46314037 intron variant T/A;C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs17034950
rs17034950
1 1.000 0.120 2 46311655 intron variant G/A snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs1867784
rs1867784
1 1.000 0.120 2 46307081 intron variant T/C snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs1867785
rs1867785
1 1.000 0.120 2 46307199 intron variant A/G snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs1867787
rs1867787
1 1.000 0.120 2 46298252 intron variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2034327
rs2034327
1 1.000 0.120 2 46321901 intron variant G/C snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs2044456
rs2044456
1 1.000 0.120 2 46319177 intron variant A/G snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs2346417
rs2346417
1 1.000 0.120 2 46301822 intron variant T/A snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs4952818
rs4952818
1 1.000 0.120 2 46309917 intron variant C/T snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs4953340
rs4953340
1 1.000 0.120 2 46320925 intron variant C/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs4953345
rs4953345
1 1.000 0.120 2 46325462 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs9973653
rs9973653
1 1.000 0.120 2 46320970 intron variant G/T snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs12617313
rs12617313
2 0.925 0.120 2 46332637 intron variant A/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs9679290
rs9679290
2 0.925 0.120 2 46330505 intron variant G/C snv 0.41 0.010 1.000 1 2012 2012