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: rs121908655
rs121908655
TNFRSF11A
1 1.000 0.120 18 62358328 missense variant A/G snv 0.800 1.000 1 2008 2008
dbSNP: rs121908656
rs121908656
TNFRSF11A
1 1.000 0.120 18 62359956 missense variant T/C snv 4.0E-06 0.800 1.000 1 2008 2008
dbSNP: rs121908658
rs121908658
TNFRSF11A
1 1.000 0.120 18 62361793 stop gained G/T snv 0.800 1.000 1 2008 2008
dbSNP: rs121908659
rs121908659
TNFRSF11A
1 1.000 0.120 18 62348249 missense variant G/A;C snv 4.0E-06 0.800 1.000 1 2008 2008
dbSNP: rs121908657
rs121908657
TNFRSF11A
1 1.000 0.120 18 62354492 missense variant C/T snv 0.700 1.000 1 2008 2008