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: rs4132601
rs4132601
9 0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 0.820 1.000 4 2009 2019
dbSNP: rs11978267
rs11978267
9 0.763 0.240 7 50398606 intron variant A/G snv 0.25 0.810 1.000 5 2009 2019
dbSNP: rs6964969
rs6964969
4 0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 0.800 1.000 1 2013 2013
dbSNP: rs12669559
rs12669559
3 1.000 0.120 7 50368079 synonymous variant T/G snv 0.35 0.32 0.700 1.000 1 2013 2013
dbSNP: rs12719039
rs12719039
1 1.000 0.120 7 50351251 intron variant T/C snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs7806674
rs7806674
1 1.000 0.120 7 50356265 intron variant C/A;G snv 0.700 1.000 1 2013 2013