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: rs121917815
rs121917815
3 0.925 0.120 3 186854303 missense variant C/T snv 4.0E-06; 1.2E-05 0.700 1.000 1 2000 2000
dbSNP: rs876661321
rs876661321
1 3 186841714 upstream gene variant G/T snv 0.700 0