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: rs227060
rs227060 		0.882 0.160 11 108334154 intron variant C/T snv 0.27
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs227061
rs227061 		1.000 0.040 11 108334602 intron variant A/G snv 0.52
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs227073
rs227073 		11 108341965 intron variant G/A;C;T snv
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs227077
rs227077 		11 108382525 intron variant C/A;T snv
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs3092993
rs3092993 		0.827 0.040 11 108364388 intron variant C/A snv 0.11
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs3092993
rs3092993 		0.827 0.040 11 108364388 intron variant C/A snv 0.11
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs3092993
rs3092993 		0.827 0.040 11 108364388 intron variant C/A snv 0.11
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs3092993
rs3092993 		0.827 0.040 11 108364388 intron variant C/A snv 0.11
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs3092993
rs3092993 		0.827 0.040 11 108364388 intron variant C/A snv 0.11
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs34005627
rs34005627 		11 108430128 intron variant TTTTTTTT/-;TT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT delins 0.36
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs373759
rs373759 		0.882 0.120 11 108349930 intron variant C/T snv 0.27
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs373759
rs373759 		0.882 0.120 11 108349930 intron variant C/T snv 0.27
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs373759
rs373759 		0.882 0.120 11 108349930 intron variant C/T snv 0.27
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs419716
rs419716 		11 108350372 intron variant A/C;T snv
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs4237579
rs4237579 		11 108408474 intron variant A/G snv 0.54
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018
dbSNP: rs573890
rs573890 		11 108380636 intron variant C/G;T snv 0.53
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs609429
rs609429 		1.000 0.080 11 108325782 intron variant G/C;T snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs652311
rs652311 		0.882 0.080 11 108369342 intron variant G/A snv 0.54
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2013 2013
dbSNP: rs652311
rs652311 		0.882 0.080 11 108369342 intron variant G/A snv 0.54
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2013 2013
dbSNP: rs652311
rs652311 		0.882 0.080 11 108369342 intron variant G/A snv 0.54
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2013 2013
dbSNP: rs7121112
rs7121112 		11 108426681 intron variant T/A;C;G snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs73008229
rs73008229 		0.882 0.080 11 108316962 intron variant G/A snv 0.11
CUI: C0153535
Disease: Malignant melanoma of skin of upper limb
Malignant melanoma of skin of upper limb 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs73008229
rs73008229 		0.882 0.080 11 108316962 intron variant G/A snv 0.11
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs73008229
rs73008229 		0.882 0.080 11 108316962 intron variant G/A snv 0.11
CUI: C0153536
Disease: Malignant melanoma of skin of lower limb
Malignant melanoma of skin of lower limb 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7931930
rs7931930 		11 108397559 intron variant G/T snv 0.49
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011