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: rs2738783
rs2738783
11 0.763 0.160 20 63677259 intron variant T/G snv 0.85 0.700 1.000 1 2019 2019
dbSNP: rs3208007
rs3208007
2 1.000 0.080 20 63690935 synonymous variant T/C;G snv 0.74 0.700 1.000 1 2018 2018