Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 23
rs886424
LINC00243
0.744 0.250 6 30814225 non coding transcript exon variant C/T snp 7.1E-02 9.1E-02 16
rs13107325
SLC39A8
1.000 0.036 4 102267552 missense variant C/A,T snp 4.0E-06; 4.5E-02 4.3E-02 14
rs1006737
CACNA1C
0.679 0.107 12 2236129 intron variant G/A snp 0.37 13
rs7903146
TCF7L2
0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 13
rs8321
ZNRD1
0.734 0.250 6 30064745 3 prime UTR variant A/C snp 5.4E-02 6.5E-02 13
rs3129817 0.724 0.286 6 30374976 intergenic variant G/A snp 0.12 12
rs2524005 0.821 0.036 6 29931900 intron variant G/A snp 0.17 11
rs4650608 0.801 0.036 1 78772330 intergenic variant T/C snp 0.31 11
rs10275045
MAD1L1
0.801 0.143 7 1881190 intron variant C/T snp 0.33 11
rs1480380 0.744 0.321 6 32945469 intron variant C/T snp 0.11 10
rs17693963 0.821 0.036 6 27742386 intergenic variant A/C,G snp 6.4E-02 10
rs17746001 0.821 0.036 4 179734472 intergenic variant C/T snp 4.4E-02 10
rs9834970 0.821 0.036 3 36814539 intergenic variant T/C snp 0.44 10
rs4356203
PIK3C2A
0.821 0.036 11 17138601 intron variant A/G snp 0.33 10
rs7872515
SPTLC1
0.821 0.036 9 92060258 intron variant G/A snp 0.24 10
rs7219021
TTLL6
0.821 0.036 17 48763179 intron variant T/G snp 0.24 10
rs4949526 0.846 0.036 1 29959372 intergenic variant T/C snp 0.56 9
rs12201676 0.821 0.036 6 89022382 intergenic variant T/C snp 0.21 8
rs3782886
BRAP
0.784 0.250 12 111672685 synonymous variant T/C snp 1.9E-02 1.4E-02 8
rs802568
CNTNAP2
0.821 0.036 7 146262151 intron variant T/G snp 0.16 8
rs11789399
LOC105376249
0.801 0.036 9 118597008 intergenic variant G/A,C snp 0.35 8
rs11191580
NT5C2
0.821 0.036 10 103146454 intron variant T/C snp 8.2E-02 8
rs17782313 0.734 0.250 18 60183864 intergenic variant T/C snp 0.23 7
rs9275524 0.784 0.143 6 32707332 intergenic variant T/C snp 0.57 7