Source: ALL

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: rs10118757
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2013 2013
dbSNP: rs10118757
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2009 2009
dbSNP: rs10118757
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2009 2009
dbSNP: rs10118757
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2013 2013
dbSNP: rs10118757
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2009 2009
dbSNP: rs10118757
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 < 0.001 1 2013 2013
dbSNP: rs10757257
rs10757257
MTAP
0.882 0.080 9 21806565 intron variant G/A snv 0.34
CUI: C0334424
Disease: Nodular melanoma
Nodular melanoma 		0.010 1.000 1 2011 2011
dbSNP: rs10757257
rs10757257
MTAP
0.882 0.080 9 21806565 intron variant G/A snv 0.34
CUI: C2739810
Disease: Lentigo maligna melanoma
Lentigo maligna melanoma 		0.010 1.000 1 2011 2011
dbSNP: rs7023329
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.010 1.000 1 2017 2017
dbSNP: rs7023329
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.010 1.000 1 2013 2013
dbSNP: rs7023329
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		0.010 1.000 1 2013 2013
dbSNP: rs7023329
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		0.010 1.000 1 2013 2013
dbSNP: rs7023329
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2011 2011
dbSNP: rs7023329
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		0.010 1.000 1 2013 2013
dbSNP: rs7023329
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2011 2011
dbSNP: rs7023954
rs7023954
MTAP
0.925 0.040 9 21816759 missense variant G/A snv 0.40 0.42
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 2016 2016
dbSNP: rs7027989
rs7027989
MTAP
0.925 0.120 9 21817755 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2009 2009
dbSNP: rs869329
rs869329
MTAP
0.851 0.080 9 21804694 intron variant A/G;T snv
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 2019 2019
dbSNP: rs869330
rs869330
MTAP
0.925 0.080 9 21804618 intron variant A/G snv 0.62
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 2019 2019
dbSNP: rs869330
rs869330
MTAP
0.925 0.080 9 21804618 intron variant A/G snv 0.62
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		0.010 1.000 1 2019 2019
dbSNP: rs10118757
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.020 1.000 2 2012 2013
dbSNP: rs10811625
rs10811625
MTAP
1.000 0.040 9 21826841 intron variant G/A;T snv
CUI: C0027960
Disease: Nevus
Nevus 		0.700 1.000 1 2009 2009
dbSNP: rs10965144
rs10965144
MTAP
1.000 0.040 9 21808914 5 prime UTR variant C/T snv 0.36
CUI: C0027960
Disease: Nevus
Nevus 		0.700 1.000 1 2009 2009
dbSNP: rs11532907
rs11532907
MTAP
0.882 0.080 9 21844773 intron variant A/G;T snv
CUI: C0153535
Disease: Malignant melanoma of skin of upper limb
Malignant melanoma of skin of upper limb 		0.700 1.000 1 2018 2018
dbSNP: rs11532907
rs11532907
MTAP
0.882 0.080 9 21844773 intron variant A/G;T snv
CUI: C0153536
Disease: Malignant melanoma of skin of lower limb
Malignant melanoma of skin of lower limb 		0.700 1.000 1 2018 2018