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: rs786200925
rs786200925
WNT5A
2 0.925 0.200 3 55479457 missense variant C/G snv 0.700 1.000 1 2010 2010
dbSNP: rs786204836
rs786204836
WNT5A
2 0.925 0.200 3 55479448 missense variant T/C snv 0.700 1.000 1 2015 2015
dbSNP: rs869312850
rs869312850
WNT5A
1 1.000 0.200 3 55474476 missense variant C/G snv 0.700 1.000 1 2010 2010