Disease: Serum albumin measurement
Source: ALL
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 81
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 6
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 4
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs1440581
PPM1K-DT
1.000 0.080 4 88305270 intron variant T/A;C snv 4
rs1912826
KLKB1
4 186228386 intron variant G/A;C snv 4
rs2657880
SPRYD4
12 56469986 3 prime UTR variant G/C snv 0.15 4
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 3
rs16850360 4 74006728 intron variant A/G snv 4.2E-02 2
rs16939881
ALDH1A2 ; AQP9
15 58179780 intron variant G/C;T snv 2
rs712964 22 19168604 upstream gene variant T/C snv 0.66 2