Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs2270916
CASR
0.851 0.120 3 122282252 intron variant T/C snv 0.13 0.11 6
rs10222633
CASR
0.925 0.080 3 122258079 intron variant G/A snv 0.45 4
rs10934578
CASR
0.925 0.080 3 122258435 intron variant G/T snv 0.30 4
rs12485716
CASR
0.925 0.080 3 122260843 intron variant G/A snv 0.36 2
rs17250717
CASR
0.925 0.080 3 122261339 intron variant G/T snv 7.4E-02 2
rs1802757
CASR
0.925 0.080 3 122286284 3 prime UTR variant C/T snv 0.17 2
rs3804592
CASR
0.925 0.080 3 122260382 intron variant G/A snv 0.18 2
rs4678174
CASR
0.925 0.080 3 122282024 intron variant C/T snv 0.56 2
rs6918698
CCN2
0.851 0.200 6 131952117 intron variant G/A;C snv 5
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 16
rs35187787
CDH1
0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 6
rs2737
CDK5RAP3
0.851 0.080 17 47981705 missense variant T/C snv 0.25 0.19 4
rs1289280947
CDKN2A
0.851 0.080 9 21974571 missense variant C/T snv 4.0E-06 5
rs774904310
CDKN2A
0.925 0.080 9 21971055 frameshift variant C/- delins 3
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs2059691
CHROMR ; PRKRA
0.882 0.080 2 178437157 intron variant A/G snv 0.72 3
rs1440032367
COL11A2
0.925 0.080 6 33189169 missense variant G/C snv 7.0E-06 3
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46