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: rs10808026
rs10808026
2 1.000 0.080 7 143402040 intron variant C/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs3935067
rs3935067
1 1.000 0.080 7 143407238 intron variant G/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs56402156
rs56402156
1 1.000 0.080 7 143406388 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018