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: rs11568350
rs11568350
SLC40A1
9 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2012 2012
dbSNP: rs2076101
rs2076101
APOBEC3F
3 0.925 0.080 22 39049549 missense variant G/A snv 0.52 0.44 0.010 1.000 1 2016 2016
dbSNP: rs2243250
rs2243250
IL4
61 0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs3204849
rs3204849
CCRL2 ; CCR5AS
1 1.000 0.080 3 46408579 missense variant T/A snv 0.38 0.31 0.010 1.000 1 2011 2011
dbSNP: rs891403796
rs891403796
DHPS
1 1.000 0.080 19 12681601 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2012 2012