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: rs4141819
rs4141819
2 1.000 0.040 2 67637543 intron variant C/T snv 0.71 0.820 1.000 3 2012 2015