Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs3024321
F13A1
6 6317893 intron variant A/G snv 0.29 2
rs7766109
F13A1
1.000 0.120 6 6256600 intron variant G/A snv 0.63 2
rs10484323
F13A1
6 6271953 intron variant T/C snv 0.13 1
rs11243078
F13A1
6 6316569 intron variant T/G snv 0.15 1
rs12333289
F13A1
6 6263213 intron variant C/T snv 0.13 1
rs12664620
F13A1
6 6282710 intron variant A/G snv 0.31 1
rs1475072
F13A1
6 6313264 intron variant C/T snv 0.73 1
rs1674043
F13A1
6 6310383 intron variant T/A snv 0.77 1
rs1674045
F13A1
6 6310955 intron variant A/C;G snv 1
rs17141966
F13A1
6 6272392 intron variant T/C snv 0.13 1
rs17378819
F13A1
6 6307210 intron variant T/C snv 0.16 1
rs1742932
F13A1
6 6304298 intron variant G/A;T snv 1
rs1742934
F13A1
6 6308517 intron variant A/C snv 0.34 1
rs1742937
F13A1
6 6309465 intron variant G/A snv 0.34 1
rs1781790
F13A1
6 6314349 intron variant G/C snv 0.78 1
rs2755413
F13A1
6 6310303 intron variant T/C snv 0.79 1
rs2755416
F13A1
6 6311468 intron variant A/G;T snv 1
rs3024317
F13A1
6 6319146 intron variant G/A snv 0.45 1
rs3024339
F13A1
6 6314660 intron variant T/C snv 7.3E-02 1
rs3024342
F13A1
6 6314410 intron variant T/C snv 0.15 1
rs3024370
F13A1
6 6250734 intron variant G/A snv 0.34 1
rs3024371
F13A1
6 6250679 intron variant T/A snv 0.20 1
rs3851514
F13A1
6 6274337 intron variant T/C snv 0.74 1
rs3863221
F13A1
6 6259349 intron variant T/A snv 0.72 1