Source: BEFREE

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: rs10139403
rs10139403
DLK1
1.000 0.040 14 100728224 intron variant A/G snv 0.62
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.010 1.000 1 2016 2016
dbSNP: rs1802710
rs1802710
DLK1
14 100734308 synonymous variant T/A;C snv 0.63
CUI: C0024299
Disease: Lymphoma
Lymphoma 		0.010 1.000 1 2004 2004
dbSNP: rs1802710
rs1802710
DLK1
14 100734308 synonymous variant T/A;C snv 0.63
CUI: C4317171
Disease: Adolescent Obesity
Adolescent Obesity 		0.010 1.000 1 2008 2008
dbSNP: rs1802710
rs1802710
DLK1
14 100734308 synonymous variant T/A;C snv 0.63
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		0.010 1.000 1 2004 2004
dbSNP: rs2295660
rs2295660
DLK1
1.000 0.080 14 100734443 synonymous variant T/C snv 1.1E-02 1.2E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2007 2007
dbSNP: rs770804393
rs770804393
DLK1
0.882 0.240 14 100734514 missense variant G/A snv 4.0E-06 7.0E-06
CUI: C0010073
Disease: Coronary Artery Vasospasm
Coronary Artery Vasospasm 		0.010 1.000 1 2002 2002
dbSNP: rs770804393
rs770804393
DLK1
0.882 0.240 14 100734514 missense variant G/A snv 4.0E-06 7.0E-06
CUI: C0520680
Disease: Sleep Apnea, Central
Sleep Apnea, Central 		0.010 1.000 1 2002 2002
dbSNP: rs770804393
rs770804393
DLK1
0.882 0.240 14 100734514 missense variant G/A snv 4.0E-06 7.0E-06
CUI: C0751039
Disease: Cockayne Syndrome, Type I
Cockayne Syndrome, Type I 		0.010 1.000 1 2002 2002