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: rs2255141
rs2255141
10 112174128 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs2255141
rs2255141
10 112174128 intron variant A/G;T snv
Low density lipoprotein cholesterol measurement
0.800 1.000 3 2010 2018
dbSNP: rs2297991
rs2297991
10 112153464 3 prime UTR variant T/C snv 0.69
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 4 2015 2019
dbSNP: rs1129555
rs1129555
10 112150963 3 prime UTR variant A/G snv 0.71
Low density lipoprotein cholesterol measurement
0.700 1.000 3 2015 2018
dbSNP: rs1129555
rs1129555
10 112150963 3 prime UTR variant A/G snv 0.71
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 3 2017 2019
dbSNP: rs2255141
rs2255141
10 112174128 intron variant A/G;T snv
High density lipoprotein measurement
0.700 1.000 3 2018 2019
dbSNP: rs1129555
rs1129555
10 112150963 3 prime UTR variant A/G snv 0.71
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs2255141
rs2255141
10 112174128 intron variant A/G;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 2 2010 2013
dbSNP: rs7096937
rs7096937
10 112190660 intron variant T/C snv 0.72
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs7096937
rs7096937
10 112190660 intron variant T/C snv 0.72
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs7096937
rs7096937
10 112190660 intron variant T/C snv 0.72
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs7096937
rs7096937
10 112190660 intron variant T/C snv 0.72
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs77147124
rs77147124
10 112159366 intron variant A/G snv
High density lipoprotein measurement
0.700 1.000 2 2015 2018
dbSNP: rs10787429
rs10787429
10 112189906 intron variant T/A;C snv
Alanine aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs10787429
rs10787429
10 112189906 intron variant T/A;C snv
Serum Alanine Aminotransferase Measurement
0.700 1.000 1 2018 2018
dbSNP: rs1129555
rs1129555
10 112150963 3 prime UTR variant A/G snv 0.71
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1129555
rs1129555
10 112150963 3 prime UTR variant A/G snv 0.71
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs2255141
rs2255141
10 112174128 intron variant A/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs2297991
rs2297991
10 112153464 3 prime UTR variant T/C snv 0.69
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs2297991
rs2297991
10 112153464 3 prime UTR variant T/C snv 0.69
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs2297991
rs2297991
10 112153464 3 prime UTR variant T/C snv 0.69
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs2792735
rs2792735
10 112162067 intron variant G/A snv 0.77
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs2803621
rs2803621
10 112179826 intron variant G/A snv 0.74
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs2803621
rs2803621
10 112179826 intron variant G/A snv 0.74
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs2803621
rs2803621
10 112179826 intron variant G/A snv 0.74
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018