Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10519210 1.000 0.040 15 63445726 intergenic variant T/C;G snv 1
rs11172782 1.000 0.040 12 58865846 intergenic variant A/G snv 0.12 1
rs1520832 1.000 0.040 12 42859612 regulatory region variant T/C;G snv 1
rs4528684 1.000 0.040 19 14240762 intergenic variant C/T snv 0.12 1
rs548097 1.000 0.040 13 75202132 intergenic variant G/C;T snv 1
rs2210327
ADAMTSL1
1.000 0.040 9 18109237 intron variant A/T snv 3.4E-02 1
rs12638540
CMTM7
1.000 0.040 3 32447042 intron variant A/G;T snv 1
rs2125623
OTUD7A
1.000 0.040 15 31537504 intron variant C/T snv 0.33 1
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs10932374
ERBB4
0.925 0.040 2 211379678 3 prime UTR variant G/A snv 0.23 2
rs13003941
ERBB4
0.925 0.040 2 211378978 3 prime UTR variant G/C;T snv 0.26 2
rs1595064
ERBB4
0.925 0.040 2 211378020 3 prime UTR variant G/A;C snv 2
rs1595065
ERBB4
0.925 0.040 2 211377916 3 prime UTR variant G/A snv 0.73 2
rs3748960
ERBB4
0.925 0.040 2 211383109 3 prime UTR variant C/T snv 0.96 2
rs6787362
FRMD4B
0.925 0.040 3 69178228 intron variant A/G snv 9.3E-02 2
rs6123837
GNAS ; LOC101927932
0.925 0.040 20 58890516 synonymous variant G/A snv 0.30 2
rs2241562
HRH2
0.925 0.040 5 175684809 intron variant G/C;T snv 1.0E-03 2
rs1429117513
LAG3
0.925 0.040 12 6775316 synonymous variant T/C snv 4.0E-06 2
rs1337916669
LOC108783645 ; HFE
0.925 0.040 6 26092879 missense variant G/T snv 2
rs34376731
PPP1R1A
0.925 0.040 12 54581014 missense variant C/T snv 4.6E-03 1.9E-02 2
rs9303504
PRKCA
0.925 0.040 17 66319248 intron variant G/C snv 0.59 2
rs9909004
PRKCA
0.925 0.040 17 66310015 intron variant C/T snv 0.59 2
rs3212247
RIPK3
0.925 0.040 14 24340589 upstream gene variant A/G snv 0.12 2
rs3212254
RIPK3 ; ADCY4
0.925 0.040 14 24336257 missense variant G/A;T snv 1.2E-05; 7.3E-02 2
rs1805126
SCN5A
0.925 0.040 3 38550915 synonymous variant A/G snv 0.39 0.44 2