Gene: F11 ×
Source: GWASDB ×
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: rs2036914
rs2036914
F11
2 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.830 1.000 1 2011 2019
dbSNP: rs3756008
rs3756008
F11
2 4 186264231 upstream gene variant A/T snv 0.36 0.810 1.000 2 2011 2014
dbSNP: rs4253399
rs4253399
F11
2 4 186266940 intron variant T/G snv 0.30 0.800 1.000 2 2011 2013
dbSNP: rs4253417
rs4253417
F11
2 4 186277851 intron variant T/C;G snv 0.800 1.000 1 2011 2019
dbSNP: rs925451
rs925451
F11
2 4 186266415 intron variant G/A snv 0.34 0.710 1.000 2 2010 2012
dbSNP: rs3756009
rs3756009
F11
2 4 186264957 upstream gene variant A/G snv 0.32 0.700 1.000 2 2011 2012
dbSNP: rs1593
rs1593
F11
3 4 186274397 3 prime UTR variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs4241824
rs4241824
F11
2 4 186270633 intron variant G/A snv 0.55 0.700 1.000 1 2011 2011