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: rs12877501
rs12877501
COL4A2
4 0.925 0.160 13 110512039 missense variant G/A;C snv 5.0E-04 0.700 0
dbSNP: rs121918697
rs121918697
THRB
4 0.882 0.040 3 24127631 missense variant G/A snv 0.010 1.000 1 2011 2011
dbSNP: rs1360780
rs1360780
FKBP5 ; LOC112267956
31 0.708 0.320 6 35639794 intron variant T/A;C snv 0.010 1.000 1 2019 2019