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: rs12765002
rs12765002
2 1.000 0.040 10 102875591 intron variant C/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs3740393
rs3740393
10 0.776 0.280 10 102876898 intron variant G/C;T snv 0.700 1.000 1 2018 2018