Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 3
rs6585827
PLEKHA1
1.000 0.040 10 122406099 intron variant G/A snv 0.47 3
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 3
rs10801551 1.000 0.040 1 196610909 upstream gene variant G/A;C snv 2
rs10922144 1.000 0.040 1 196854170 intron variant C/A;T snv 2
rs10922146 1.000 0.040 1 196865506 intron variant C/T snv 0.19 2
rs12029571 1.000 0.040 1 196634172 intergenic variant A/G snv 0.24 2
rs12047098 1.000 0.040 1 196865976 intron variant T/C snv 0.19 2
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs1963605 1.000 0.040 1 196853038 intron variant C/A;T snv 2
rs1964645 1.000 0.040 1 196852884 intron variant T/A;C snv 2
rs4657825 1.000 0.040 1 196615191 intergenic variant A/G;T snv 2
rs6657442 1.000 0.040 1 196868930 intron variant T/C snv 0.19 2
rs7413265 1.000 0.040 1 196870033 intron variant G/T snv 0.19 2
rs7555070 1.000 0.040 1 197013024 downstream gene variant C/T snv 0.57 2
rs493258
ALDH1A2
0.925 0.040 15 58395681 intron variant T/C snv 0.50 2
rs920915
ALDH1A2
1.000 0.040 15 58396268 intron variant C/G snv 0.55 2
rs1042663
C2 ; CYP21A2 ; C2-AS1
0.925 0.160 6 31937353 synonymous variant G/A snv 9.7E-02 0.12 2
rs550605
C2 ; CYP21A2 ; C2-AS1
0.925 0.160 6 31939370 intron variant T/C snv 9.7E-02 0.12 2
rs541862
CFB ; CYP21A2
0.882 0.160 6 31949174 non coding transcript exon variant T/C snv 0.12 2
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 2
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 2
rs10801560
CFH
1.000 0.040 1 196745470 intron variant C/A snv 0.19 2
rs10801561
CFH
1.000 0.040 1 196745540 intron variant T/A snv 0.19 2