IGF2, insulin like growth factor 2, 3481

N. diseases: 604; N. variants: 19
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: rs2585
rs2585
11 2129214 3 prime UTR variant T/C;G snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs35506085
rs35506085
11 2144346 intron variant G/A snv 0.17
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs35506085
rs35506085
11 2144346 intron variant G/A snv 0.17
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs35506085
rs35506085
11 2144346 intron variant G/A snv 0.17
CUI: C0424678
Disease: Lean body mass
Lean body mass
0.700 1.000 1 2019 2019
dbSNP: rs3741205
rs3741205
11 2148654 non coding transcript exon variant C/A;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs3741210
rs3741210
11 2148310 non coding transcript exon variant A/G snv 0.30
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs3741210
rs3741210
11 2148310 non coding transcript exon variant A/G snv 0.30
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs7948458
rs7948458
11 2151600 intron variant A/C snv 0.76
CUI: C0005910
Disease: Body Weight
Body Weight
Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2018 2018
dbSNP: rs975030738
rs975030738
11 2135469 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs869320620
rs869320620
1.000 11 2135501 stop gained G/A;T snv 4.0E-06
GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES
0.700 0
dbSNP: rs1003483
rs1003483
1.000 0.040 11 2146313 non coding transcript exon variant T/G snv 0.47 0.40
CUI: C0271183
Disease: Severe myopia
Severe myopia
Eye Diseases 0.010 1.000 1 2015 2015
dbSNP: rs149483638
rs149483638
1.000 0.080 11 2140300 splice acceptor variant C/T snv 2.8E-02 1.5E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs3741211
rs3741211
0.925 0.080 11 2147880 non coding transcript exon variant A/G snv 0.36
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2011 2011
dbSNP: rs3741211
rs3741211
0.925 0.080 11 2147880 non coding transcript exon variant A/G snv 0.36
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2011 2011
dbSNP: rs680
rs680
0.925 0.080 11 2132404 3 prime UTR variant T/C;G snv 0.78
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs680
rs680
0.925 0.080 11 2132404 3 prime UTR variant T/C;G snv 0.78
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs984257990
rs984257990
0.925 0.080 11 2135495 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs984257990
rs984257990
0.925 0.080 11 2135495 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs984257990
rs984257990
0.925 0.080 11 2135495 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1064794050
rs1064794050
1.000 0.080 11 2135446 stop gained G/A;C snv
CUI: C0175693
Disease: Russell-Silver syndrome
Russell-Silver syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 0
dbSNP: rs1114167321
rs1114167321
1.000 0.080 11 2135365 splice donor variant -/GC delins
CUI: C0175693
Disease: Russell-Silver syndrome
Russell-Silver syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 0
dbSNP: rs4320932
rs4320932
0.882 0.120 11 2150371 intron variant T/C snv 0.19
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 1.000 2 2011 2013
dbSNP: rs4320932
rs4320932
0.882 0.120 11 2150371 intron variant T/C snv 0.19
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 1.000 2 2011 2013
dbSNP: rs4320932
rs4320932
0.882 0.120 11 2150371 intron variant T/C snv 0.19
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 1.000 2 2011 2013
dbSNP: rs3741208
rs3741208
1.000 0.120 11 2148544 non coding transcript exon variant A/G;T snv
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.800 1.000 1 2007 2007