Source: ALL

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: rs2228468
rs2228468
ACKR2 ; CYP8B1 ; KRBOX1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 3 2013 2018
dbSNP: rs2228468
rs2228468
ACKR2 ; CYP8B1 ; KRBOX1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 3 2013 2018
dbSNP: rs2228467
rs2228467
ACKR2 ; CYP8B1 ; KRBOX1
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 2 2013 2016
dbSNP: rs2228467
rs2228467
ACKR2 ; CYP8B1 ; KRBOX1
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 2 2013 2016
dbSNP: rs2228467
rs2228467
ACKR2 ; CYP8B1 ; KRBOX1
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs11715464
rs11715464
ACKR2 ; CYP8B1 ; KRBOX1
3 42868195 intron variant A/G snv 0.28
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs1366046
rs1366046
ACKR2 ; CYP8B1 ; KRBOX1
3 42867283 3 prime UTR variant A/C snv 0.36
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs2195224
rs2195224
ACKR2 ; CYP8B1 ; KRBOX1
3 42859508 intron variant G/A;C snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs2195224
rs2195224
ACKR2 ; CYP8B1 ; KRBOX1
3 42859508 intron variant G/A;C snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs2228467
rs2228467
ACKR2 ; CYP8B1 ; KRBOX1
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2014 2014
dbSNP: rs2228467
rs2228467
ACKR2 ; CYP8B1 ; KRBOX1
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs2228467
rs2228467
ACKR2 ; CYP8B1 ; KRBOX1
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2228467
rs2228467
ACKR2 ; CYP8B1 ; KRBOX1
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2228467
rs2228467
ACKR2 ; CYP8B1 ; KRBOX1
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02
CUI: C4318750
Disease: Chemokine (C-C Motif) Ligand 19 Measurement
Chemokine (C-C Motif) Ligand 19 Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2228468
rs2228468
ACKR2 ; CYP8B1 ; KRBOX1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs3919627
rs3919627
ACKR2 ; CYP8B1 ; KRBOX1
3 42867668 intron variant G/A snv 0.36
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3919627
rs3919627
ACKR2 ; CYP8B1 ; KRBOX1
3 42867668 intron variant G/A snv 0.36
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs4682863
rs4682863
ACKR2 ; KRBOX1
3 42836219 intron variant A/G snv 0.45
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4682868
rs4682868
ACKR2 ; CYP8B1 ; KRBOX1
3 42864023 intron variant A/T snv 0.40
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7612912
rs7612912
ACKR2 ; CYP8B1 ; KRBOX1
3 42869129 intron variant T/C snv 0.39
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs9815043
rs9815043
ACKR2 ; KRBOX1
3 42855147 intron variant A/G snv 0.37
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs9872440
rs9872440
ACKR2 ; KRBOX1
3 42854959 intron variant T/C;G snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs9872570
rs9872570
ACKR2 ; KRBOX1
3 42855023 intron variant T/A snv 0.37
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs9872570
rs9872570
ACKR2 ; KRBOX1
3 42855023 intron variant T/A snv 0.37
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9872570
rs9872570
ACKR2 ; KRBOX1
3 42855023 intron variant T/A snv 0.37
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016