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: rs2275085
rs2275085
1 1 45620180 3 prime UTR variant C/T snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs3014240
rs3014240
1 1 45623553 splice region variant C/G snv 0.70 0.73 0.700 1.000 1 2019 2019