Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs371074389
LOC112268426 ; CXCR4
0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs766914563
LOC112268426 ; CXCR4
0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs2228014
CXCR4
0.752 0.240 2 136115514 synonymous variant G/A snv 4.6E-02 3.5E-02 14
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs104893626
CXCR4 ; LOC112268426
0.827 0.280 2 136114915 stop gained G/C snv 11
rs770327175
CXCR4
0.851 0.120 2 136115878 missense variant C/A;T snv 8.0E-06 5
rs910532454
CXCR4
0.882 0.080 2 136115453 missense variant C/A;T snv 4.0E-06 4
rs147198552
CXCR4
0.882 0.080 2 136115450 missense variant C/T snv 1.2E-05 7.0E-06 3
rs104893624
LOC112268426 ; CXCR4
0.851 0.200 2 136114928 stop gained G/A snv 3
rs756207760
CXCR4
2 136115275 missense variant C/G;T snv 4.0E-06; 4.0E-06 2
rs769772228
CXCR4
0.925 0.080 2 136115346 missense variant C/G snv 2.0E-05 4.9E-05 2
rs1194919682
CXCR4 ; LOC112268426
0.925 0.040 2 136115158 missense variant A/G snv 2
rs553062694
CXCR4
1.000 0.080 2 136116611 intron variant C/T snv 6.7E-04 1
rs1333957805
CXCR4
1.000 0.040 2 136115639 missense variant C/T snv 1
rs764148917
CXCR4
2 136115282 synonymous variant G/A snv 4.0E-06 1
rs375868851
CXCR4
1.000 0.040 2 136115889 synonymous variant G/A;C snv 5.2E-05; 8.0E-06 1
rs2471859
CXCR4
1.000 0.040 2 136116434 intron variant A/G snv 0.31 1
rs1272938495
CXCR4 ; LOC112268426
1.000 2 136115225 missense variant G/A snv 4.0E-06 7.0E-06 1