Source: INFERRED ×
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: rs3732858
rs3732858
1 3 43056273 missense variant G/A snv 0.19 0.14 0.700 1.000 1 2018 2018
dbSNP: rs62247124
rs62247124
1 3 43039458 intron variant T/C snv 0.18 0.700 1.000 1 2019 2019