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: rs1148247
rs1148247
3 0.882 0.160 10 35208018 intron variant G/A snv 0.33 0.010 1.000 1 2012 2012
dbSNP: rs12775799
rs12775799
1 1.000 0.040 10 35199336 intron variant C/T snv 0.33 0.010 1.000 1 2012 2012
dbSNP: rs16935888
rs16935888
1 1.000 0.040 10 35143477 intron variant T/C snv 0.15 0.010 1.000 1 2012 2012
dbSNP: rs4934735
rs4934735
1 1.000 0.040 10 35207802 intron variant A/G snv 0.33 0.010 1.000 1 2012 2012
dbSNP: rs6481941
rs6481941
1 1.000 0.040 10 35151213 intron variant G/A snv 0.37 0.010 1.000 1 2012 2012