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: rs5996696
rs5996696
1 1.000 0.040 22 24431654 intron variant A/C snv 0.12 0.010 1.000 1 2011 2011
dbSNP: rs71651683
rs71651683
1 1.000 0.040 22 24432885 5 prime UTR variant C/T snv 3.6E-02 0.010 1.000 1 2011 2011