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: rs3750081
rs3750081
1 7 32891264 intron variant T/G snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs3750082
rs3750082
2 7 32880315 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016