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: rs398124645
rs398124645
TAF2
1 1.000 8 119783548 missense variant A/G snv 0.800 1.000 2 2011 2013
dbSNP: rs398124655
rs398124655
TAF2
1 1.000 8 119793396 missense variant G/T snv 0.700 1.000 2 2011 2013
dbSNP: rs398124656
rs398124656
TAF2
1 1.000 8 119803881 missense variant G/A;C snv 0.700 1.000 2 2011 2013