Source: ALL
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: rs2294021
rs2294021
CCDC22
8 0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 0.010 1.000 1 2018 2018
dbSNP: rs2609255
rs2609255
FAM13A
4 0.882 0.080 4 88890044 intron variant G/T snv 0.73 0.010 1.000 1 2017 2017
dbSNP: rs3761547
rs3761547
FOXP3
3 0.882 0.200 X 49262004 intron variant T/C snv 9.6E-02 0.010 1.000 1 2018 2018
dbSNP: rs3761549
rs3761549
FOXP3
18 0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 0.010 1.000 1 2018 2018