Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs4129767
PGS1
17 78407903 intron variant G/A snv 0.46 6
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 6
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51 6
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 5
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 5