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: rs3923564
rs3923564
2 1.000 0.040 10 79976225 intron variant A/G snv 5.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs7078012
rs7078012
2 1.000 0.040 10 79945677 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012