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: rs12998782
rs12998782
3 0.882 0.160 2 118967804 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs13389814
rs13389814
1 1.000 0.040 2 118984374 intron variant A/G snv 0.11 0.010 1.000 1 2013 2013
dbSNP: rs4491733
rs4491733
1 1.000 0.040 2 118960452 intron variant A/G snv 0.37 0.010 1.000 1 2013 2013
dbSNP: rs6751745
rs6751745
2 0.925 0.080 2 118983428 intron variant C/T snv 0.31 0.010 1.000 1 2016 2016
dbSNP: rs7559955
rs7559955
1 1.000 0.040 2 118967393 intron variant C/G;T snv 0.010 1.000 1 2013 2013