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: rs12037861
rs12037861
HLX-AS1
1 220864835 intron variant A/T snv 0.28
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs12141189
rs12141189
HLX ; HLX-AS1
1 220880203 missense variant T/C snv 0.24 0.23
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs17597773
rs17597773
HLX ; HLX-AS1
1 220881419 non coding transcript exon variant C/G snv 0.25 0.23
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs17597773
rs17597773
HLX ; HLX-AS1
1 220881419 non coding transcript exon variant C/G snv 0.25 0.23
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2131887
rs2131887
HLX-AS1
1.000 0.040 1 220834513 intron variant T/C snv 0.61
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2453237
rs2453237
HLX-AS1
1 220855242 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs41369048
rs41369048
HLX ; HLX-AS1
1 220878224 intron variant A/G snv 9.7E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs41369048
rs41369048
HLX ; HLX-AS1
1 220878224 intron variant A/G snv 9.7E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016