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: rs28722705
rs28722705
ANKRD55
5 56158115 intron variant A/T snv 9.9E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs28722705
rs28722705
ANKRD55
5 56158115 intron variant A/T snv 9.9E-02
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs28722705
rs28722705
ANKRD55
5 56158115 intron variant A/T snv 9.9E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2014 2019
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015
dbSNP: rs71624119
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 3 2012 2017
dbSNP: rs71624119
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 2 2015 2016
dbSNP: rs71624119
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs71624119
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs71624119
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs71624119
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs71624119
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016