Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12972990
ICAM5
1.000 0.040 19 10295755 intron variant T/G snv 0.35 1
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 1
rs13708
STX1B ; HSD3B7
1.000 0.040 16 30989488 3 prime UTR variant G/A;C snv 0.52 1
rs142903734
LOC107987207
1.000 0.040 14 98202442 intron variant GA/-;GAGA delins 1
rs144098432
POLI
1.000 0.040 18 54290024 intron variant C/T snv 0.25 1
rs1576
CCHCR1
1.000 0.040 6 31142614 missense variant G/A;C snv 4.0E-06; 0.28 1
rs1581803 1.000 0.040 1 152619805 downstream gene variant G/T snv 0.58 1
rs17052344
UBBP4
1.000 0.040 17 22190937 intron variant G/A snv 0.19 1
rs191667458
USP49
1.000 0.040 6 41829160 intron variant G/A;T snv 1
rs1975974
UBBP4
1.000 0.040 17 22180454 intron variant A/G snv 0.18 1
rs2076346
ELOA-AS1 ; ELOA
1.000 0.040 1 23757159 intron variant T/C snv 0.27 0.21 1
rs2276405
AIM2
1.000 0.040 1 159073406 stop gained C/A;T snv 8.0E-06; 1.5E-02 1
rs2295359
C1orf141 ; IL23R
1.000 0.040 1 67170267 intron variant G/A snv 0.32 1
rs240993
MFSD4B ; REV3L
1.000 0.040 6 111352511 intron variant T/A;C snv 1
rs2455826
BTD
1.000 0.040 3 15621553 intron variant G/T snv 0.26 1
rs2476847
EXOC2
1.000 0.040 6 549390 intron variant C/T snv 0.44 1
rs249038
ZFYVE16
1.000 0.040 5 80449650 missense variant A/G snv 0.91 0.87 1
rs2700987
ELMO1
1.000 0.040 7 37346633 intron variant C/A snv 0.60 1
rs2724013
ELMO1
1.000 0.040 7 37349706 intron variant G/A;T snv 1
rs2781377
SYNE2 ; ESR2
1.000 0.040 14 64093374 stop gained G/A snv 8.5E-02 8.9E-02 1
rs28512356
TP63
1.000 0.040 3 189897686 downstream gene variant C/A;G snv 1
rs2853694
IL12B ; LOC107986469
0.925 0.040 5 159322080 intron variant G/A;T snv 1
rs28624578
KLF13 ; LOC105376707
1.000 0.040 15 31345463 intron variant T/C snv 0.12 1
rs3174808
LOC107985481 ; DONSON ; SON
1.000 0.040 21 33573415 missense variant T/A;C snv 4.0E-06; 0.32 1
rs34394770
COG6
1.000 0.040 13 39759232 intron variant T/C snv 0.29 1