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: rs4862848
rs4862848
1 1.000 0.120 4 188000286 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6837349
rs6837349
1 1.000 0.120 4 188000201 intron variant G/A;T snv 0.700 1.000 1 2017 2017