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: rs11599176
rs11599176
2 0.925 0.080 10 67894017 intron variant A/G snv 0.11 0.010 1.000 1 2018 2018
dbSNP: rs33957861
rs33957861
3 0.882 0.160 10 67887218 intron variant C/T snv 0.11 0.010 1.000 1 2018 2018