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: rs3804133
rs3804133
3 0.925 0.120 6 25552640 intron variant C/T snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs407934
rs407934
3 0.925 0.120 6 25504334 intron variant C/T snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs572657
rs572657
2 0.925 0.120 6 25512919 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs6903765
rs6903765
4 0.925 0.120 6 25609510 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs6908390
rs6908390
4 0.925 0.120 6 25609528 intron variant C/T snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs742132
rs742132
4 0.925 0.120 6 25607343 intron variant A/G snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs7761700
rs7761700
4 0.925 0.120 6 25617963 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs969297
rs969297
3 0.925 0.120 6 25543411 intron variant G/A snv 0.82 0.700 1.000 1 2013 2013