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: rs741702
rs741702
1 19 12913436 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs8012
rs8012
2 19 12899706 3 prime UTR variant A/G snv 0.61 0.64 0.700 1.000 1 2016 2016