Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 4
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs6741751
TRPM8
0.925 0.040 2 233919016 intron variant G/A snv 7.8E-02 3
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs6478241
ASTN2
0.925 0.040 9 116490350 intron variant A/G;T snv 2
rs11759769
FHL5
1.000 0.040 6 96617336 downstream gene variant G/A snv 0.18 2
rs422951
NOTCH4
0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 2
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs4379368
SUGCT
0.925 0.040 7 40426601 intron variant C/T snv 0.12 2
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 2
rs10737909 1 15222140 upstream gene variant G/T snv 0.45 1
rs10849061 12 4414290 intergenic variant C/T snv 0.43 1
rs10915437 1.000 0.040 1 4122946 intergenic variant A/G snv 0.29 1
rs11624776 14 93129246 regulatory region variant A/C;T snv 1
rs12136856 1 156503322 upstream gene variant C/G snv 0.54 1
rs16904191 8 130021250 upstream gene variant A/G snv 0.36 1
rs17303101 9 116419515 intergenic variant G/A snv 0.27 1
rs2074193 1.000 0.040 12 47377646 non coding transcript exon variant T/G snv 0.21 1