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: rs752504125
rs752504125
FOXF1
1 1.000 16 86511227 missense variant G/A;T snv 7.7E-06 0.700 1.000 1 1990 1990
dbSNP: rs137852660
rs137852660
FGF8
3 0.882 0.160 10 101775209 missense variant G/A snv 1.1E-03 8.0E-04 0.010 1.000 1 2014 2014