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: rs28441202
rs28441202
2 0.925 0.120 1 152156387 missense variant A/G snv 0.010 1.000 1 2017 2017
dbSNP: rs3001978
rs3001978
3 0.882 0.160 1 152153991 3 prime UTR variant T/C snv 0.50 0.010 1.000 1 2017 2017