Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11923427
RAF1
0.925 0.080 3 12622336 intron variant C/G;T snv 2
rs1238788540
BRAF
0.925 0.080 7 140800368 missense variant G/C snv 4.0E-06 7.0E-06 2
rs12485716
CASR
0.925 0.080 3 122260843 intron variant G/A snv 0.36 2
rs12490683
LOC105377207 ; MYLKP1
0.925 0.080 3 75329934 non coding transcript exon variant G/A snv 0.46 2
rs12497343
MYLKP1 ; LOC105377207
0.925 0.080 3 75330074 intron variant C/G;T snv 2
rs12591359
MIR4713HG ; CYP19A1
0.925 0.080 15 51247171 intron variant G/A snv 0.41 2
rs1287152741
DHFR
0.925 0.080 5 80633984 missense variant C/T snv 8.0E-06 1.4E-05 2
rs1365611 0.925 0.080 4 174462542 intergenic variant C/T snv 0.28 2
rs1390282714
MAPK1
0.925 0.080 22 21769233 missense variant C/A;T snv 4.0E-06; 4.0E-06 2
rs1425164489
TCN2
0.925 0.080 22 30617374 missense variant A/G;T snv 4.0E-06 2
rs1450640054
IGFBP3
0.925 0.080 7 45921122 missense variant T/C snv 1.0E-05 2
rs17109924
LGR5
0.925 0.080 12 71584007 missense variant T/C snv 7.4E-02 8.6E-02 2
rs1724120
ASTL ; DUSP2
0.925 0.080 2 96143592 3 prime UTR variant T/C snv 0.53 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
rs1967327
PRKRA ; PJVK
0.925 0.080 2 178449632 intron variant G/A;C;T snv 2
rs202011365
IL4 ; LOC105379176
0.925 0.080 5 132679748 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 2
rs2099902
MBL2
0.925 0.080 10 52766089 3 prime UTR variant T/C snv 0.33 2
rs2243828
MPO
0.925 0.080 17 58281523 upstream gene variant A/G;T snv 2
rs2302313
EPX ; MKS1
0.925 0.080 17 58205665 3 prime UTR variant G/A snv 9.2E-02 8.3E-02 2
rs2332897 0.925 0.080 4 174465154 intergenic variant C/A;G snv 0.29 2
rs2470144
CYP19A1
0.925 0.080 15 51329528 intron variant T/C snv 0.60 2
rs283415
ADH1C ; ADH1B
0.925 0.080 4 99349450 intron variant C/T snv 0.64 2
rs374400
OBSCN
0.925 0.080 1 228347383 intron variant C/T snv 0.40 2
rs3744400
ELP5 ; CLDN7
0.925 0.080 17 7260404 synonymous variant A/C;G snv 4.1E-02; 8.0E-06; 4.0E-06 2.4E-02 2