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: rs13300483
rs13300483
DELEC1
1.000 0.080 9 114881082 intron variant C/T snv 0.21
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 2 2015 2016
dbSNP: rs10817688
rs10817688
DELEC1
1.000 0.040 9 114943689 intron variant A/G snv 0.39
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs10817688
rs10817688
DELEC1
1.000 0.040 9 114943689 intron variant A/G snv 0.39
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2015 2015
dbSNP: rs10817758
rs10817758
DELEC1
1.000 0.040 9 115381654 intron variant C/T snv 0.13
CUI: C0023343
Disease: Leprosy
Leprosy 		0.700 1.000 1 2015 2015
dbSNP: rs10982456
rs10982456
TNFSF8 ; DELEC1
9 114928478 intron variant T/C snv 0.57
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10982544
rs10982544
TNC ; DELEC1
9 115114784 intron variant T/C snv 4.6E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs112106319
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2016 2016
dbSNP: rs112106319
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.700 1.000 1 2016 2016
dbSNP: rs112106319
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2016 2016
dbSNP: rs1138545
rs1138545
TNC ; DELEC1
1.000 9 115073620 missense variant C/A;T snv 0.12
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12376870
rs12376870
DELEC1 ; LOC101928748
9 115128288 intron variant G/A snv 0.18
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1250023
rs1250023
TNC ; DELEC1
9 115107651 intron variant C/T snv 0.41
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1330349
rs1330349
TNC ; DELEC1
1.000 0.040 9 115078463 intron variant G/A;C snv
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		0.700 1.000 1 2019 2019
dbSNP: rs2480930
rs2480930
TNC ; DELEC1
1.000 0.040 9 115080028 intron variant A/G snv 0.59
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		0.700 1.000 1 2018 2018
dbSNP: rs3181348
rs3181348
TNFSF8 ; DELEC1
9 114931904 intron variant G/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs3181348
rs3181348
TNFSF8 ; DELEC1
9 114931904 intron variant G/A;C snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs35157100
rs35157100
DELEC1 ; LOC101928748
9 115138015 intron variant A/-;AA;AAA delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs35796756
rs35796756
DELEC1 ; LOC105376232
1.000 0.080 9 115355120 intron variant G/A;C snv
CUI: C0021603
Disease: Sleep Initiation and Maintenance Disorders
Sleep Initiation and Maintenance Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs3833490
rs3833490
TNC ; DELEC1
9 115117849 intron variant T/-;TT;TTT delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4979467
rs4979467
DELEC1
0.925 0.080 9 114867763 intron variant C/T snv 0.52
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2017 2017
dbSNP: rs4979503
rs4979503
DELEC1 ; LOC101928748
9 115139787 intron variant G/A;C snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs57814325
rs57814325
TNC ; DELEC1
9 115117689 intron variant G/A snv 0.22
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs726657
rs726657
DELEC1
0.827 0.120 9 114934056 intron variant C/T snv 0.50
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs726657
rs726657
DELEC1
0.827 0.120 9 114934056 intron variant C/T snv 0.50
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs726657
rs726657
DELEC1
0.827 0.120 9 114934056 intron variant C/T snv 0.50
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016