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: rs267606812
rs267606812
FHL1
1 1.000 X 136207828 missense variant A/G;T snv 0.800 1.000 3 2008 2009
dbSNP: rs267606813
rs267606813
FHL1
1 1.000 X 136207829 missense variant C/G snv 0.800 1.000 3 2008 2009
dbSNP: rs122458142
rs122458142
FHL1
2 1.000 X 136207827 missense variant C/T snv 0.800 0
dbSNP: rs122458143
rs122458143
FHL1
2 1.000 X 136207855 missense variant G/T snv 0.800 0
dbSNP: rs122459146
rs122459146
FHL1
1 1.000 X 136207909 missense variant G/A snv 0.800 0