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: rs387906945
rs387906945
GDF3
1 1.000 12 7690059 missense variant A/C;G snv 5.7E-04 0.800 1.000 1 2010 2010
dbSNP: rs146973734
rs146973734
GDF3
1 1.000 12 7690389 missense variant C/T snv 1.9E-04 1.8E-04 0.800 0