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: rs2278426
rs2278426
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 3 2018 2019
dbSNP: rs4804155
rs4804155
19 11223619 intron variant C/G snv 0.18
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2017 2019
dbSNP: rs737337
rs737337
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs12979813
rs12979813
19 11232027 intron variant A/G snv 0.30
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2019 2019
dbSNP: rs17699089
rs17699089
19 11233119 intron variant A/G snv 0.15
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2019 2019