HLX, H2.0 like homeobox, 3142

N. diseases: 28; N. variants: 6
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11588625
rs11588625
1 220885504 downstream gene variant T/C snv 0.13
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12141189
rs12141189
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
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
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: rs3738182
rs3738182
1 220884320 synonymous variant G/A snv 0.18 0.20
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs41369048
rs41369048
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
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
dbSNP: rs2184658
rs2184658
0.925 0.120 1 220879115 intron variant C/G snv 0.20
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
Endocrine System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2184658
rs2184658
0.925 0.120 1 220879115 intron variant C/G snv 0.20
CUI: C0018213
Disease: Graves Disease
Graves Disease
Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2012 2012