RASGRP1, RAS guanyl releasing protein 1, 10125

N. diseases: 110; N. variants: 11
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: rs7403531
rs7403531
1.000 0.080 15 38530704 intron variant T/C;G snv 0.77
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.820 1.000 2 2013 2015
dbSNP: rs8032939
rs8032939
1.000 0.120 15 38541832 intron variant T/C snv 0.41
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 3 2014 2019
dbSNP: rs8043085
rs8043085
1.000 0.120 15 38535939 intron variant G/T snv 0.25
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs11073333
rs11073333
1.000 0.080 15 38528446 intron variant G/A snv 0.76
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs11073337
rs11073337
0.851 0.040 15 38555562 intron variant A/C snv 0.27
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs11073337
rs11073337
0.851 0.040 15 38555562 intron variant A/C snv 0.27
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2019 2019
dbSNP: rs11073337
rs11073337
0.851 0.040 15 38555562 intron variant A/C snv 0.27
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2019 2019
dbSNP: rs11073337
rs11073337
0.851 0.040 15 38555562 intron variant A/C snv 0.27
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2019 2019
dbSNP: rs11073337
rs11073337
0.851 0.040 15 38555562 intron variant A/C snv 0.27
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4924273
rs4924273
1.000 0.080 15 38554537 intron variant G/C snv 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs72727394
rs72727394
0.925 0.160 15 38554821 intron variant C/T snv 0.17
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs72727394
rs72727394
0.925 0.160 15 38554821 intron variant C/T snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs11631591
rs11631591
1.000 0.080 15 38558061 intron variant T/C snv 0.41
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4465567
rs4465567
1.000 0.080 15 38506045 intron variant T/C snv 0.32
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs4567661
rs4567661
1.000 0.080 15 38493913 non coding transcript exon variant A/C snv 0.33
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs7170151
rs7170151
1.000 0.120 15 38554477 intron variant C/T snv 0.40
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2016 2016