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: rs10769979
rs10769979
1 11 8989112 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11042149
rs11042149
1 11 8989190 intron variant T/C snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs1123936
rs1123936
1 11 8981759 3 prime UTR variant A/G snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs1980428
rs1980428
1 11 8988950 intron variant C/T snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs1980429
rs1980429
1 11 8988927 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6486060
rs6486060
2 11 9003083 intron variant G/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs7925728
rs7925728
1 11 8991455 intron variant A/G snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs7930026
rs7930026
1 11 8992092 intron variant T/A;C snv 0.700 1.000 1 2012 2012