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: rs2305929
rs2305929
4 1.000 0.040 2 27891044 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs3736594
rs3736594
3 2 27772914 intron variant A/C snv 0.62 0.700 1.000 1 2012 2012