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: rs12188167
rs12188167
1 1.000 0.040 5 88370488 intron variant C/G snv 0.15 0.700 1.000 1 2018 2018