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: rs3802954
rs3802954
1 1.000 0.040 11 60470665 3 prime UTR variant T/C snv 6.0E-02 0.010 1.000 1 2012 2012
dbSNP: rs4939364
rs4939364
1 1.000 0.040 11 60464852 intron variant A/G snv 0.66 0.010 1.000 1 2012 2012
dbSNP: rs7126354
rs7126354
1 1.000 0.040 11 60463593 intron variant C/T snv 0.64 0.010 1.000 1 2012 2012