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: rs2239222
rs2239222
1 14 72545177 intron variant A/G snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs2526932
rs2526932
2 14 72614360 downstream gene variant A/G snv 0.65 0.700 1.000 1 2013 2013