rs4969170, LOC101928674

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.020 1.000 2 2012 2018
Asthma
CUI: C0004096
Disease: Asthma
1536 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2015 2015
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2015 2015
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2018 2018
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2013 2013
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
2 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2018 2018
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2012 2012
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2015 2015
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2012 2012
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2012 2012
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 0.010 1.000 1 2015 2015