Disease: Serum LDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7666097
KDR
4 55124971 intron variant T/A;C snv 5
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02 4
rs16880248
CNR1
6 88141968 3 prime UTR variant G/T snv 2.7E-02 5
rs17513478
RIPK1
6 3101321 intron variant G/A snv 5.7E-03 5
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs9341059
ESR1
6 152097101 intron variant C/A;T snv 4
rs9465848
CDKAL1
6 20635589 intron variant C/T snv 9.3E-03 4
rs10271556
NAMPT
7 106258428 intron variant C/T snv 5.6E-02 4
rs10107815
MSRA
8 10156645 intron variant G/C snv 5.1E-02 4
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs35381288
ADRB3
8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs7000184
BAG4 ; LSM1
8 38176676 5 prime UTR variant C/T snv 2.3E-02 5
rs7001567
MSRA
8 10257027 intron variant C/G snv 3.7E-02 4
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs11568767
TGFBR1
9 99132990 intron variant C/T snv 3.7E-03 4