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: rs1537372
rs1537372
14 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1537376
rs1537376
2 1.000 0.040 9 22116221 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs2891168
rs2891168
5 0.851 0.160 9 22098620 intron variant A/G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs10116277
rs10116277
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.010 1.000 1 2011 2011
dbSNP: rs6475606
rs6475606
5 0.882 0.080 9 22081851 intron variant C/T snv 0.62 0.700 1.000 1 2011 2011