MIR6886, microRNA 6886, 102465534

N. diseases: 6; N. variants: 286
Disease: Hypercholesterolemia result ×
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: rs552422789
rs552422789 		0.925 0.080 19 11113308 missense variant G/A;C snv 1.6E-05
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs5933
rs5933 		0.925 0.080 19 11113414 missense variant C/G;T snv 3.2E-04
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs730882098
rs730882098 		0.925 0.080 19 11111586 missense variant A/C snv 8.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs730882103
rs730882103 		0.925 0.080 19 11113686 stop gained A/G;T snv 1.2E-05
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs730882106
rs730882106 		0.882 0.080 19 11113752 missense variant C/A;T snv 8.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs745343524
rs745343524 		0.925 0.080 19 11113392 missense variant C/A;G;T snv 4.0E-06; 8.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs750649426
rs750649426 		0.925 0.080 19 11111629 stop gained C/A snv 4.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs755154048
rs755154048 		0.925 0.080 19 11113705 missense variant C/T snv 1.6E-05
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs755667663
rs755667663 		1.000 0.080 19 11113678 missense variant C/A;T snv 8.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs765696008
rs765696008 		0.925 0.080 19 11113268 intron variant G/A;C snv 2.8E-05; 4.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs768430352
rs768430352 		0.925 0.080 19 11111556 missense variant G/A;C snv 1.2E-05
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs775924858
rs775924858 		0.925 0.080 19 11113450 splice donor variant G/A;T snv
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs778424518
rs778424518 		1.000 0.080 19 11113312 missense variant C/A;T snv 2.0E-05
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs781362878
rs781362878 		1.000 0.080 19 11113767 splice region variant G/A;C snv 3.2E-05; 1.6E-05
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs869025453
rs869025453 		0.925 0.080 19 11113652 frameshift variant CT/- delins 7.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs869320651
rs869320651 		0.925 0.080 19 11113343 stop gained G/A;T snv 4.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254774
rs879254774 		0.925 0.080 19 11111513 splice acceptor variant G/A;C snv
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254778
rs879254778 		1.000 0.080 19 11111520 frameshift variant A/- del
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254781
rs879254781 		0.925 0.080 19 11111522 missense variant G/A;C snv
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254786
rs879254786 		0.925 0.080 19 11111538 frameshift variant A/- del
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254790
rs879254790 		0.925 0.080 19 11111552 frameshift variant CTCTGC/GT delins
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254791
rs879254791 		0.925 0.080 19 11111555 missense variant T/C;G snv 4.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254796
rs879254796 		0.925 0.080 19 11111570 missense variant G/A;T snv 4.0E-06
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254797
rs879254797 		0.925 0.080 19 11111571 missense variant G/A;C;T snv
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0
dbSNP: rs879254800
rs879254800 		0.925 0.080 19 11111577 missense variant A/C;G snv
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		0.700 0