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: rs2524123
rs2524123
5 0.925 0.040 6 31297537 intron variant T/C snv 0.34 0.700 1.000 2 2009 2010
dbSNP: rs2894207
rs2894207
8 0.882 0.160 6 31295974 intron variant T/C snv 0.20 0.700 1.000 2 2009 2010
dbSNP: rs9366778
rs9366778
7 0.925 0.120 6 31301396 intron variant G/A snv 0.47 0.700 1.000 2 2009 2010
dbSNP: rs13191519
rs13191519
4 1.000 6 31297975 intron variant T/C snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs13216197
rs13216197
4 1.000 6 31303241 intron variant T/C snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs16899205
rs16899205
4 1.000 6 31298584 intron variant A/G snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs16899207
rs16899207
4 1.000 6 31298610 intron variant A/G snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs2247056
rs2247056
11 0.882 0.160 6 31297713 intron variant T/C snv 0.80 0.700 1.000 1 2009 2009
dbSNP: rs2394967
rs2394967
4 1.000 6 31301352 intron variant G/A snv 7.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs28367646
rs28367646
4 1.000 6 31300555 intron variant A/C snv 0.36 0.700 1.000 1 2010 2010
dbSNP: rs2853926
rs2853926
4 1.000 6 31295274 intron variant A/G snv 0.26 0.700 1.000 1 2010 2010
dbSNP: rs3873379
rs3873379
5 0.925 0.120 6 31294392 intron variant T/C snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs3873380
rs3873380
4 1.000 6 31294661 intron variant C/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs3905495
rs3905495
4 1.000 6 31297762 intron variant G/A snv 0.39 0.700 1.000 1 2010 2010
dbSNP: rs4523128
rs4523128
4 1.000 6 31301605 non coding transcript exon variant T/C snv 7.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs9380238
rs9380238
5 1.000 6 31299841 intron variant A/G snv 0.15 0.700 1.000 1 2010 2010
dbSNP: rs9468932
rs9468932
4 1.000 6 31297046 intron variant G/A snv 0.19 0.700 1.000 1 2009 2009