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: rs13085139
rs13085139
1 3 194357284 3 prime UTR variant T/G snv 1.7E-05 0.700 1.000 1 2018 2018
dbSNP: rs57514363
rs57514363
1 3 194367198 intron variant T/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs923931
rs923931
1 3 194364318 intron variant G/A;T snv 0.700 1.000 1 2018 2018