Gene: F11 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1593
rs1593
F11
3 4 186274397 3 prime UTR variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2036914
rs2036914
F11
5 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs2055916
rs2055916
F11
1 4 186275356 intron variant G/A snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs2289252
rs2289252
F11 ; F11-AS1
4 1.000 0.040 4 186286227 non coding transcript exon variant C/T snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs3756008
rs3756008
F11
2 4 186264231 upstream gene variant A/T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs3756009
rs3756009
F11
2 4 186264957 upstream gene variant A/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs3756011
rs3756011
F11
1 4 186285095 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4241824
rs4241824
F11
2 4 186270633 intron variant G/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs4253399
rs4253399
F11
2 4 186266940 intron variant T/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs4253407
rs4253407
F11
1 4 186272154 intron variant A/T snv 0.86 0.700 1.000 1 2012 2012
dbSNP: rs4253416
rs4253416
F11
2 4 186276840 intron variant C/T snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs4253417
rs4253417
F11
3 4 186277851 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs4253425
rs4253425
F11
1 4 186284775 intron variant T/A;C snv 0.91 0.700 1.000 1 2012 2012
dbSNP: rs925451
rs925451
F11
2 4 186266415 intron variant G/A snv 0.34 0.700 1.000 1 2012 2012