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: rs786205887
rs786205887
WNT3 ; LRRC37A2
1 1.000 0.120 17 46773719 missense variant A/C;G snv 0.700 0
dbSNP: rs760064852
rs760064852
LZTR1
1 1.000 0.120 22 20995986 missense variant C/T snv 0.010 1.000 1 2019 2019