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: rs11158716
rs11158716
2 14 68026441 intron variant G/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs72725174
rs72725174
1 14 68044056 intron variant C/T snv 0.13 0.700 1.000 1 2016 2016