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: rs2777899
rs2777899
4 0.851 0.160 17 59755030 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs8070345
rs8070345
1 1.000 0.080 17 59739396 intron variant T/C snv 0.41 0.700 1.000 1 2013 2013