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: rs7005606
rs7005606
3 0.925 0.080 8 32543983 intron variant T/G snv 0.39 0.700 1.000 2 2014 2016
dbSNP: rs16879552
rs16879552
3 0.882 0.080 8 32553698 intron variant C/T snv 0.10 0.700 1.000 1 2009 2009