ADAM10, ADAM metallopeptidase domain 10, 102

N. diseases: 224; N. variants: 27
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: rs11638416
rs11638416 		15 58598915 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16940571
rs16940571 		15 58590593 3 prime UTR variant C/T snv 3.5E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17269425
rs17269425 		15 58639141 intron variant A/G snv 2.1E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs347118
rs347118 		15 58708424 intron variant G/A snv 3.5E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs347122
rs347122 		15 58747033 intron variant T/C snv 3.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs387005
rs387005 		15 58717866 intron variant T/C snv 3.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4238331
rs4238331 		15 58719934 intron variant T/G snv 0.63
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs424346
rs424346 		15 58718763 intron variant C/T snv 3.5E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs437549
rs437549 		15 58731360 intron variant T/A snv 3.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs602921
rs602921 		15 58711735 intron variant C/T snv 3.5E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs793417
rs793417 		15 58703238 intron variant T/C snv 3.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.030 0.667 3 2012 2018
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.020 1.000 2 2015 2019
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.020 1.000 2 2015 2019
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2015 2015
dbSNP: rs653765
rs653765 		0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs514049
rs514049 		0.827 0.160 15 58750164 intron variant C/A snv 0.57
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.030 0.667 3 2012 2018
dbSNP: rs514049
rs514049 		0.827 0.160 15 58750164 intron variant C/A snv 0.57
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs514049
rs514049 		0.827 0.160 15 58750164 intron variant C/A snv 0.57
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs514049
rs514049 		0.827 0.160 15 58750164 intron variant C/A snv 0.57
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018