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: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2018 2018
dbSNP: rs2817040
rs2817040
ARMC12 ; LOC285847
2 6 35737829 intron variant G/A snv 0.22 0.010 1.000 1 2013 2013
dbSNP: rs7734804
rs7734804
LOC105377703
2 5 164919530 intron variant G/T snv 8.3E-02 0.010 1.000 1 2018 2018