Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs2844615
HLA-B
1.000 6 31275182 intron variant C/T snv 0.11 5
rs9380238
LOC112267902 ; HLA-B ; LINC02571
1.000 6 31299841 intron variant A/G snv 0.15 5
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 4
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs10498725
CARMIL1
1.000 0.040 6 25454787 intron variant C/T snv 0.17 3
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 3
rs12449157
GFOD2
1.000 0.040 16 67674994 3 prime UTR variant A/G snv 0.30 3
rs12669559
IKZF1
1.000 0.120 7 50368079 synonymous variant T/G snv 0.35 0.32 3
rs17563986
MAPT
1.000 0.040 17 45913906 intron variant A/G snv 0.14 3
rs1981997
MAPT
1.000 0.040 17 45979401 non coding transcript exon variant G/A snv 0.14 3
rs2668692
KANSL1
1.000 0.040 17 46215654 intron variant G/A;T snv 3
rs415430
WNT3 ; LRRC37A2
1.000 0.040 17 46781778 intron variant C/T snv 0.84 3
rs422112
LINC02210-CRHR1 ; LINC02210
1.000 0.080 17 45650771 non coding transcript exon variant G/A snv 0.14 3
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 3
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 3
rs7215239
LINC02210-CRHR1
1.000 0.040 17 45690407 intron variant T/C snv 0.30 3
rs8176722
ABO
1.000 0.040 9 133257367 intron variant C/A snv 0.13 0.12 3
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 3
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 2
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 2
rs1033500
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32339605 missense variant G/A snv 0.40 0.33 2
rs10445338
MAPT
1.000 0.040 17 45990316 intron variant G/A snv 0.15 2
rs10445364
MAPT-AS1
1.000 0.040 17 45838990 intron variant G/A;C snv 2