Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs308379
FGF2
1.000 0.080 4 122861741 intron variant A/T snv 0.68 2
rs3771300
STAT1
1.000 0.080 2 190970870 intron variant T/G snv 0.47 2
rs3816747
DLC1
1.000 0.080 8 13499293 missense variant G/A snv 0.87 0.89 2
rs39315
CFTR ; WNT2
1.000 0.080 7 117323508 intron variant T/C;G snv 2
rs4945008
NADSYN1
1.000 0.080 11 71510202 intron variant A/G;T snv 2
rs57408770
MIR3131 ; IHH
1.000 0.080 2 219058688 non coding transcript exon variant -/AAG delins 2
rs587776802
PIK3CA
1.000 0.080 3 179234358 frameshift variant -/A delins 2
rs7116978
PDE3B
1.000 0.080 11 14860225 intron variant T/C snv 0.65 2
rs7708357 1.000 0.080 5 177104771 intergenic variant A/G snv 0.58 2
rs778624338
CTNNB1
1.000 0.080 3 41227270 stop gained C/A;T snv 2.0E-05 7.0E-06 2
rs7959378
TFCP2
1.000 0.080 12 51173447 upstream gene variant A/C snv 0.41 2
rs7976497
MLEC
1.000 0.080 12 120697664 3 prime UTR variant T/C snv 0.60 2
rs8191246
HSD17B2
1.000 0.080 16 82098435 stop lost A/G snv 1.3E-02 1.9E-02 2
rs894151
C8orf37-AS1
1.000 0.080 8 95226180 intron variant T/C snv 0.39 2
rs9200
C6 ; LOC105374739
1.000 0.080 5 41142504 3 prime UTR variant C/A;T snv 2
rs9926344
WWOX
1.000 0.080 16 78986883 intron variant G/A;C;T snv 2
rs10052999
C6
1.000 0.080 5 41165642 intron variant C/T snv 7.5E-02 1
rs1049112
PRR4 ; PRH1-PRR4 ; PRH2 ; PRH1
1.000 0.080 12 10930757 missense variant A/G;T snv 0.11; 1.4E-05 1
rs1053096
NPAS2
1.000 0.080 2 100996153 3 prime UTR variant T/C snv 0.61 1
rs1057519982
TP53
1.000 0.080 17 7674239 missense variant A/C;G;T snv 1
rs1065403
SCD5
1.000 0.080 4 82629966 3 prime UTR variant T/C snv 0.63 1
rs10773771
PIWIL1
1.000 0.080 12 130371771 3 prime UTR variant C/T snv 0.50 1
rs10789859
SDHD
1.000 0.080 11 112089809 intron variant T/C snv 0.31 1
rs1081432 1.000 0.080 2 6708412 intergenic variant T/C snv 1
rs111904020
STAT3
1.000 0.080 17 42314141 3 prime UTR variant A/C snv 1