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: rs7977418
rs7977418
3 12 28435309 intron variant T/C snv 0.40 0.700 1.000 2 2019 2019
dbSNP: rs2348418
rs2348418
2 12 28536581 intron variant T/C snv 0.40 0.700 1.000 1 2017 2017