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: rs121908450
rs121908450
RANBP2 ; EDAR
4 0.851 0.160 2 108929288 missense variant C/T snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs121908452
rs121908452
RANBP2 ; EDAR
2 0.925 0.080 2 108897182 stop gained G/A snv 0.700 0
dbSNP: rs121908453
rs121908453
RANBP2 ; EDAR
3 0.882 0.080 2 108896995 missense variant C/T snv 0.700 0
dbSNP: rs121908456
rs121908456
RANBP2 ; EDAR
1 1.000 2 108897194 stop gained C/A;T snv 0.700 0