Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1042713
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2009 2009
dbSNP: rs1042714
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2009 2009
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2019 2019
dbSNP: rs13222905
rs13222905
GIMAP4
0.882 0.160 7 150566901 upstream gene variant G/A snv 0.15
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2015 2015
dbSNP: rs1801275
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2009 2009
dbSNP: rs2251746
rs2251746
FCER1A
0.882 0.120 1 159302270 intron variant T/C snv 0.20
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2008 2008
dbSNP: rs2289278
rs2289278
TSLP
0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2016 2016
dbSNP: rs2427837
rs2427837
FCER1A
0.851 0.160 1 159288755 upstream gene variant G/A snv 0.20
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2008 2008
dbSNP: rs2569190
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2010 2010
dbSNP: rs447713
rs447713
IL1RN
0.851 0.160 2 113130095 non coding transcript exon variant A/G snv 0.21
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2006 2006
dbSNP: rs4742170
rs4742170
IL33 ; LOC107987046
0.925 0.080 9 6242950 intron variant C/G;T snv
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 < 0.001 1 2018 2018
dbSNP: rs555743307
rs555743307
IL4R
0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2009 2009
dbSNP: rs6965571
rs6965571
GIMAP5 ; GIMAP1-GIMAP5
0.882 0.160 7 150737384 5 prime UTR variant G/A snv 0.18
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2015 2015
dbSNP: rs71625199
rs71625199
FLG ; FLG-AS1
1.000 1 152307488 synonymous variant C/A;T snv 8.0E-06; 2.3E-02
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2017 2017
dbSNP: rs769790595
rs769790595
IL4R
0.827 0.120 16 27360785 missense variant G/A;C snv 2.0E-05; 4.0E-06
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2009 2009
dbSNP: rs8034191
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2012 2012