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: rs4802307
rs4802307
0.827 0.120 19 46346549 upstream gene variant G/T snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.800 1.000 4 2012 2017
dbSNP: rs3764613
rs3764613
1.000 0.040 19 46392960 3 prime UTR variant A/G snv 0.50
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer
Stomatognathic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4802307
rs4802307
0.827 0.120 19 46346549 upstream gene variant G/T snv 0.21
CUI: C0033860
Disease: Psoriasis
Psoriasis
Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs4802307
rs4802307
0.827 0.120 19 46346549 upstream gene variant G/T snv 0.21
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4802307
rs4802307
0.827 0.120 19 46346549 upstream gene variant G/T snv 0.21
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs4802307
rs4802307
0.827 0.120 19 46346549 upstream gene variant G/T snv 0.21
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs4802307
rs4802307
0.827 0.120 19 46346549 upstream gene variant G/T snv 0.21
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs4803936
rs4803936
19 46375372 intron variant G/A snv 0.22
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs62136106
rs62136106
19 46365128 intron variant A/G snv 0.22
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs8106745
rs8106745
19 46388911 intron variant T/C snv 0.75
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.700 1.000 1 2019 2019