Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10756819
BNC2
1.000 0.120 9 16858086 intron variant G/A;C;T snv 1
rs12379687
BNC2
1.000 0.120 9 16854369 intron variant G/A;T snv 1
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 1
rs12937080
BRIP1
1.000 0.120 17 61852376 intron variant A/G;T snv 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 1
rs4445329 1.000 0.120 9 16911759 intergenic variant G/A;C snv 1
rs4961501
BNC2
1.000 0.120 9 16851680 intron variant T/A;C;G snv 1
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 1
rs7861573
BNC2
1.000 0.120 9 16862282 intron variant A/G;T snv 1
rs367899983
BNC2
1.000 0.120 9 16864524 intron variant GTCT/- delins 4.2E-05 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 2
rs34289250
BRIP1
0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 1
rs12938171
INTS2
1.000 0.120 17 61902994 intron variant G/A snv 9.0E-03 1
rs12451939
MED13
1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 1
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 1
rs10962656 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 2
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 1
rs10810666 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 1
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3