Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11084596 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 3
rs11199879 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 3
rs2555019 1.000 0.040 12 114230813 intergenic variant T/C;G snv 3
rs2556378
BCL11A
1.000 0.040 2 60535367 3 prime UTR variant T/G snv 0.81 3
rs381949
CLPTM1L
1.000 0.040 5 1322353 intron variant G/A snv 0.44 3
rs4548546
WDR11
1.000 0.040 10 120870067 intron variant C/G;T snv 3
rs148678804 1.000 0.040 10 22138360 intergenic variant G/A;T snv 2
rs1638703
DLEU1
1.000 0.040 13 50514220 intron variant G/C snv 0.27 2
rs200476 1.000 0.040 6 27800570 intergenic variant A/T snv 0.28 2
rs6061244
GATA5
1.000 0.040 20 62466597 intron variant G/A;C snv 1.3E-03; 0.38 2
rs6561599
DLEU1 ; RNASEH2B-AS1
1.000 0.040 13 50904782 non coding transcript exon variant C/G snv 0.61 2
rs677394
C5orf66
1.000 0.040 5 135271869 intron variant G/C;T snv 2
rs72878024
BET1L ; ODF3
1.000 0.040 11 199492 missense variant G/A snv 6.4E-02 6.4E-02 2
rs7906649 1.000 0.040 10 22021369 intergenic variant G/A snv 0.60 2
rs9958656
LOC101927548
1.000 0.040 18 22324181 intergenic variant T/A;C snv 2
rs10035432
C5orf46
1.000 0.040 5 147855193 upstream gene variant G/A snv 0.18 1
rs1047100
FGFR2
1.000 0.040 10 121538644 synonymous variant T/A;C snv 1.2E-05; 0.78 1
rs10786938 1.000 0.040 10 106280012 intergenic variant G/C;T snv 1
rs115336889
ROPN1L
1.000 0.040 5 10454257 intron variant G/A;C snv 1
rs141179786 1.000 0.040 18 53662174 intergenic variant A/G;T snv 2.2E-02 1
rs16902947 1.000 0.040 5 36308995 intergenic variant A/G snv 0.22 1
rs2710383
SYN3
1.000 0.040 22 32554983 intron variant G/C snv 0.11 1
rs36067435
ELOVL6
1.000 0.040 4 110180390 intron variant -/TTAT delins 1
rs3797177
SRD5A1
1.000 0.040 5 6666971 intron variant T/A;C snv 1
rs534957
GCLC
1.000 0.040 6 53541553 intron variant G/C snv 0.39 1