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: rs11191865
rs11191865
3 0.925 0.160 10 103913084 intron variant G/A snv 0.44 0.800 1.000 1 2013 2013
dbSNP: rs1980653
rs1980653
1 10 103894406 intron variant A/G snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs2067832
rs2067832
1 10 103883376 intron variant G/A snv 0.44 0.700 1.000 1 2013 2013