Disease: Serum albumin measurement
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 25
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 23
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 22
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 18
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 17
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 16
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 15
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 13
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 12
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 12
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 12
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 12
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 12
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 12
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 11