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: rs10174949
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.800 1.000 3 2013 2018
dbSNP: rs13008689
rs13008689
LINC00299
2 8390126 intron variant G/A snv 0.35
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2010 2010
dbSNP: rs367023
rs367023
LINC00299
1.000 0.040 2 8309993 intron variant A/G snv 0.35
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.800 1.000 1 2013 2016
dbSNP: rs10165200
rs10165200
LINC00299
2 8299499 intron variant G/A snv 0.36
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs10165200
rs10165200
LINC00299
2 8299499 intron variant G/A snv 0.36
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs10174949
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs10178845
rs10178845
LINC00299
1.000 0.080 2 8303673 intron variant G/A snv 0.23
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs10199605
rs10199605
LINC00299
1.000 0.120 2 8354967 intron variant G/A snv 0.26
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.700 1.000 1 2015 2015
dbSNP: rs13395467
rs13395467
LINC00299
1.000 0.120 2 8311368 intron variant A/G snv 0.24
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs13412757
rs13412757
LINC00299
1.000 0.080 2 8317950 intron variant G/A snv 0.29
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2016 2016
dbSNP: rs13416555
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs13416555
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs17169
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2015 2015
dbSNP: rs17169
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2015 2015
dbSNP: rs17169
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2015 2015
dbSNP: rs17169
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2015 2015
dbSNP: rs17169
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		0.700 1.000 1 2015 2015
dbSNP: rs346835
rs346835
LINC00299
2 8298563 intron variant C/T snv 0.39
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs346835
rs346835
LINC00299
2 8298563 intron variant C/T snv 0.39
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs367023
rs367023
LINC00299
1.000 0.040 2 8309993 intron variant A/G snv 0.35
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs3856439
rs3856439
LINC00299
0.925 0.080 2 8319274 intron variant C/A;T snv 0.29
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs3856439
rs3856439
LINC00299
0.925 0.080 2 8319274 intron variant C/A;T snv 0.29
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs409169
rs409169
LINC00299
2 8415954 intron variant A/G snv 0.17
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2019 2019
dbSNP: rs62106670
rs62106670
LINC00299
1.000 0.080 2 8456993 intron variant C/T snv 0.31
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs7572278
rs7572278
LINC00299
2 8422899 intron variant T/A snv 0.34
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019