Source: GWASDB

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: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.900 0.923 1 2007 2019
dbSNP: rs4977574
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.880 1.000 2 2007 2018
dbSNP: rs10738607
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.810 1.000 1 2007 2018
dbSNP: rs2383207
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.770 1.000 1 2007 2013
dbSNP: rs1333045
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.730 1.000 1 2007 2018
dbSNP: rs1333040
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.720 0.667 1 2007 2011
dbSNP: rs10116277
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2007 2007
dbSNP: rs10811650
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2007 2007
dbSNP: rs1333046
rs1333046
CDKN2B-AS1
0.925 0.080 9 22124124 intron variant T/A snv 0.43
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2007 2007
dbSNP: rs1333048
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2007 2007
dbSNP: rs6475608
rs6475608
CDKN2B-AS1
1.000 0.080 9 22101703 intron variant T/C snv 0.60
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2007 2007