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: rs35863382
rs35863382
3 1.000 0.040 14 91472532 intron variant C/T snv 6.0E-02 0.700 1.000 1 2016 2016