Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs66495454
LOC105378797 ; NEGR1
1 72282884 upstream gene variant -/TCC;TCCT ins 0.28 1
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 4
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs2393967
MIR1296 ; JMJD1C
10 63373396 intron variant A/C snv 0.23 3
rs10956838 1.000 0.040 8 92392214 intergenic variant A/C snv 0.28 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs13267290 1.000 0.040 8 110466092 intergenic variant A/C snv 0.20 2
rs2163503
ZRANB2-AS2
1 71335356 intron variant A/C snv 0.17 2
rs56116382
BSN
3 49568755 intron variant A/C snv 0.19 2
rs750472
PPP1R16A ; FOXH1
8 144476070 upstream gene variant A/C snv 0.50 2
rs10011007 4 130143535 intergenic variant A/C snv 8.3E-02 1
rs10196283
ZNF385B
2 179850608 intron variant A/C snv 0.15 1
rs10789907 11 112689091 intron variant A/C snv 0.54 1
rs10806984
DCDC2
6 24181603 intron variant A/C snv 0.35 1
rs112223196
SBK1
16 28287097 intron variant A/C snv 0.16 1
rs13089785
CCDC14
3 123935062 intron variant A/C snv 0.46 1
rs1421334
PURG
8 31008217 intron variant A/C snv 0.48 1
rs151411 4 102217471 intergenic variant A/C snv 0.22 1
rs17062018 5 163599232 intron variant A/C snv 7.7E-03 1
rs17256010 14 59896409 intergenic variant A/C snv 0.17 1
rs179994
ATXN1
6 16320756 intron variant A/C snv 0.31 1
rs1826347
BSN
3 49634221 intron variant A/C snv 0.49 1
rs1892423
FOXO6
1 41383668 downstream gene variant A/C snv 0.49 1