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: rs2395185
rs2395185
17 0.724 0.360 6 32465390 intron variant G/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9268853
rs9268853
10 0.790 0.440 6 32461866 intron variant T/C snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9268858
rs9268858
5 0.882 0.200 6 32461981 intron variant T/C snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9268923
rs9268923
2 1.000 0.040 6 32465058 intron variant C/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9268969
rs9268969
1 6 32466572 intron variant C/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9268979
rs9268979
1 6 32467267 intron variant T/C snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs9286790
rs9286790
2 1.000 0.120 6 32472051 intron variant G/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9405040
rs9405040
2 1.000 0.120 6 32471616 intron variant A/C;T snv 0.700 1.000 1 2012 2012