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: rs1345778
rs1345778
1 1.000 0.040 5 40712695 3 prime UTR variant A/C snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs2329353
rs2329353
1 1.000 0.040 5 40748166 intron variant G/A snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs3792826
rs3792826
1 1.000 0.040 5 40753775 intron variant G/A snv 5.8E-02 0.700 1.000 1 2011 2011
dbSNP: rs6868517
rs6868517
1 1.000 0.040 5 40752434 intron variant A/G snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs6882769
rs6882769
1 1.000 0.040 5 40647661 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs7716982
rs7716982
1 1.000 0.040 5 40646458 intron variant G/T snv 0.66 0.700 1.000 1 2011 2011
dbSNP: rs7730020
rs7730020
1 1.000 0.040 5 40657850 intron variant T/C snv 0.69 0.700 1.000 1 2011 2011