Gene: F2 ×
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: rs3136441
rs3136441
F2
2 11 46721697 intron variant T/C snv 0.13 0.700 1.000 2 2010 2013
dbSNP: rs2070850
rs2070850
F2
2 11 46719945 non coding transcript exon variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs3136457
rs3136457
F2
2 11 46724708 intron variant G/C snv 0.13 0.700 1.000 1 2012 2012