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: rs3922844
rs3922844
3 3 38582762 intron variant T/C snv 0.61 0.700 1.000 1 2017 2017
dbSNP: rs41312411
rs41312411
2 3 38579746 intron variant C/G snv 0.11 0.700 1.000 1 2017 2017