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: rs140756663
rs140756663
TSPYL1 ; DSE
2 0.925 0.040 6 116278733 missense variant G/T snv 3.6E-03 2.7E-03 0.010 1.000 1 2012 2012
dbSNP: rs370116569
rs370116569
TSPYL1 ; DSE
2 0.925 0.040 6 116279412 missense variant G/C snv 3.2E-05 2.1E-05 0.010 1.000 1 2012 2012