Source: GWASCAT

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: rs7937
rs7937
RAB4B ; MIA-RAB4B ; RAB4B-EGLN2
0.851 0.080 19 40796801 3 prime UTR variant C/A;T snv 0.49
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.830 1.000 2 2012 2018
dbSNP: rs17726276
rs17726276
RAB4B ; MIA-RAB4B ; RAB4B-EGLN2
19 40785214 intron variant G/A snv 0.42
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs184088518
rs184088518
EGLN2 ; RAB4B-EGLN2
19 40799233 5 prime UTR variant G/T snv 1.8E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs184088518
rs184088518
EGLN2 ; RAB4B-EGLN2
19 40799233 5 prime UTR variant G/T snv 1.8E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2604909
rs2604909
RAB4B ; MIA-RAB4B ; RAB4B-EGLN2
19 40791710 intron variant C/T snv 0.21
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs3733829
rs3733829
EGLN2 ; RAB4B-EGLN2
0.882 0.120 19 40804666 non coding transcript exon variant A/G snv 0.28
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2010 2010
dbSNP: rs61750953
rs61750953
EGLN2 ; RAB4B-EGLN2
19 40800745 missense variant C/T snv 1.6E-02 1.4E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs61750953
rs61750953
EGLN2 ; RAB4B-EGLN2
19 40800745 missense variant C/T snv 1.6E-02 1.4E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7937
rs7937
RAB4B ; MIA-RAB4B ; RAB4B-EGLN2
0.851 0.080 19 40796801 3 prime UTR variant C/A;T snv 0.49
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015