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: rs122458144
rs122458144
FHL1
1 1.000 X 136207917 missense variant T/C;G snv 0.800 0
dbSNP: rs122458145
rs122458145
FHL1
1 1.000 X 136207918 missense variant G/A snv 0.800 0
dbSNP: rs122459147
rs122459147
FHL1
1 1.000 X 136207169 missense variant T/C snv 0.800 0