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: rs17127608
rs17127608
2 1 65428258 intron variant C/T snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs9436735
rs9436735
5 1 65419378 upstream gene variant C/G snv 2.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs9436742
rs9436742
2 1 65432648 3 prime UTR variant C/T snv 2.3E-02 0.700 1.000 1 2012 2012