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: rs35628
rs35628
1 1.000 0.080 16 16077249 intron variant A/G snv 0.13 0.700 0
dbSNP: rs3888565
rs3888565
1 1.000 0.080 16 16089188 intron variant G/A snv 0.25 0.700 0
dbSNP: rs4148353
rs4148353
1 1.000 0.080 16 16077291 intron variant G/A;T snv 0.700 0