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: rs2030839
rs2030839
1 15 83915207 intron variant T/C snv 0.63 0.700 1.000 1 2017 2017
dbSNP: rs4842838
rs4842838
3 15 83913372 missense variant G/A;T snv 1.6E-05; 0.61 0.700 1.000 1 2017 2017
dbSNP: rs7162542
rs7162542
4 15 83845538 intron variant C/A;G;T snv 0.700 1.000 1 2017 2017