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: rs6671895
rs6671895
2 1.000 0.120 1 38089354 intron variant C/A;T snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs7532231
rs7532231
2 1.000 0.120 1 104193445 intron variant A/G;T snv 0.39 0.700 1.000 1 2019 2019