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: rs10510607
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs10510607
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs10510607
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs10510607
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs10510607
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs11921493
rs11921493
CMC1
0.925 0.040 3 28261297 intron variant A/C snv 4.8E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs11921493
rs11921493
CMC1
0.925 0.040 3 28261297 intron variant A/C snv 4.8E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs4502545
rs4502545
CMC1
3 28261539 intron variant G/A;T snv
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4585155
rs4585155
CMC1
3 28280095 intron variant G/A snv 0.47
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs4585155
rs4585155
CMC1
3 28280095 intron variant G/A snv 0.47
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs73822569
rs73822569
CMC1
1.000 0.080 3 28290744 intron variant A/G snv 4.4E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017