Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7849
SCD
1.000 0.080 10 100362846 3 prime UTR variant T/C;G snv 1
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs2281611
MEG8 ; MIR495
0.925 0.080 14 101033612 intron variant G/A;T snv 2
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs34713741
SELENOS
0.882 0.280 15 101277671 upstream gene variant C/A;T snv 0.24 3
rs1419316960
DNMT1
0.925 0.080 19 10166651 missense variant T/C snv 7.0E-06 2
rs823920 0.925 0.080 9 101900303 intergenic variant A/G snv 0.12 2
rs537292284
PPRC1
1.000 0.080 10 102133102 missense variant G/C snv 1
rs35060588
IRAK2
0.925 0.080 3 10213318 missense variant C/G;T snv 5.5E-02; 1.6E-05 2
rs1215486792
MOK
0.925 0.080 14 102229572 missense variant C/G snv 7.0E-06 2
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs11704
CINP ; ZNF839
0.925 0.080 14 102342318 3 prime UTR variant G/C snv 0.26 2
rs2946834
LINC02456 ; HELLPAR
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63 7
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 25
rs867538330
SLCO6A1
0.925 0.080 5 102458457 synonymous variant C/T snv 2
rs230490
LOC105377621
0.882 0.080 4 102466262 downstream gene variant G/A snv 0.34 3
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs28720239
LOC105377621 ; NFKB1
1.000 0.080 4 102500998 non coding transcript exon variant ATTG/- delins 1
rs230510
NFKB1
1.000 0.080 4 102555009 intron variant T/A snv 0.37 1
rs3821958
NFKB1
1.000 0.080 4 102587667 intron variant A/G snv 0.42 1