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: rs2076056
rs2076056
3 0.882 0.200 6 15487551 intron variant C/A;G;T snv 0.24 0.010 1.000 1 2017 2017
dbSNP: rs2237138
rs2237138
3 0.882 0.200 6 15463164 intron variant T/C snv 0.22 0.010 1.000 1 2017 2017