CDKN2B-AS1, CDKN2B antisense RNA 1, 100048912

N. diseases: 213; N. variants: 183
Disease: Myocardial Infarction ×
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: rs10757278
rs10757278 		0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.900 0.923 13 2007 2019
dbSNP: rs4977574
rs4977574 		0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.880 1.000 10 2007 2018
dbSNP: rs10738607
rs10738607 		0.925 0.080 9 22088095 intron variant A/G snv 0.42
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.810 1.000 3 2007 2018
dbSNP: rs2383207
rs2383207 		0.695 0.280 9 22115960 intron variant A/G snv 0.64
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.770 1.000 8 2007 2013
dbSNP: rs1333045
rs1333045 		0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.730 1.000 4 2007 2018
dbSNP: rs1333040
rs1333040 		0.732 0.280 9 22083405 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.720 0.667 3 2007 2011
dbSNP: rs2891168
rs2891168 		0.851 0.160 9 22098620 intron variant A/G snv 0.40
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.710 1.000 2 2010 2015
dbSNP: rs10116277
rs10116277 		0.827 0.160 9 22081398 intron variant G/T snv 0.62
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2007 2007
dbSNP: rs10811650
rs10811650 		0.882 0.200 9 22067594 intron variant A/G snv 0.37
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2007 2007
dbSNP: rs1333046
rs1333046 		0.925 0.080 9 22124124 intron variant T/A snv 0.43
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2007 2007
dbSNP: rs1333048
rs1333048 		0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2007 2007
dbSNP: rs6475608
rs6475608 		1.000 0.080 9 22101703 intron variant T/C snv 0.60
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2007 2007
dbSNP: rs1333049
rs1333049 		0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.100 1.000 15 2008 2019
dbSNP: rs10757274
rs10757274 		0.701 0.320 9 22096056 intron variant A/G snv 0.41
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.090 1.000 9 2008 2018
dbSNP: rs2383206
rs2383206 		0.742 0.320 9 22115027 intron variant A/G snv 0.49
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.040 1.000 4 2008 2012
dbSNP: rs518394
rs518394 		0.827 0.160 9 22019674 intron variant G/C snv 0.30
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2013 2019
dbSNP: rs1063192
rs1063192 		0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10738605
rs10738605 		0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10965215
rs10965215 		0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1412829
rs1412829 		0.742 0.400 9 22043927 intron variant A/G snv 0.28
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3217992
rs3217992 		0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs4977756
rs4977756 		0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs564398
rs564398 		0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7865618
rs7865618 		0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9632884
rs9632884 		0.851 0.160 9 22072302 intron variant G/A;C snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2020 2020