Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs892161
HDGFL2
19 4493711 synonymous variant A/G snv 0.61 0.62 1
rs871841
ARHGEF15
17 8313150 missense variant T/C snv 0.56 0.58 2
rs870992
ITGA1
1.000 0.080 5 52897406 intron variant A/G snv 7.9E-02 7.0E-02 2
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs826682
LIMS1
2 108615932 intron variant A/C snv 0.18 1
rs826681
LIMS1
2 108615619 intron variant C/T snv 0.17 2
rs821840
CETP
16 56959974 upstream gene variant A/G snv 4
rs8180991 8 125488108 intron variant C/G snv 0.19 2
rs8178824
APOH
17 66228657 intron variant C/T snv 2.3E-02 3
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 5
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 3
rs8102280
MAU2
19 19344941 non coding transcript exon variant G/A snv 2.8E-02 1.5E-02 3
rs8078686
KPNB1
17 47658340 intron variant T/C;G snv 0.49 3
rs8071884
PGS1
17 78401977 intron variant C/A;G;T snv 4
rs8051431
PKD1L3
16 71981352 intron variant G/A;C;T snv 1
rs8022288
SYNJ2BP ; COX16 ; SYNJ2BP-COX16
14 70380407 intron variant C/T snv 0.87 1
rs80215559
SLC17A2
6 25917997 intron variant T/C snv 3.7E-02 3
rs8017377
NYNRIN
14 24414681 missense variant G/A snv 0.37 0.34 2
rs79950627 11 2212560 intergenic variant G/A snv 2.1E-02 1
rs7968419
LOC105369969 ; CORO1C
12 108743950 regulatory region variant C/A;T snv 2
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs79588679 18 22327807 intergenic variant C/T snv 0.11 1
rs7955221 12 100456972 intergenic variant A/C;T snv 2
rs7939352
GAB2
11 78292105 intron variant G/A snv 0.27 4
rs7938117
CPT1A
11 68830586 intron variant G/A;C snv 4