Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121909209
rs121909209
0.763 0.160 5 136056781 missense variant G/A snv
CUI: C4700127
Disease: Thiel-behnke
Thiel-behnke
0.020 1.000 2 2007 2011
dbSNP: rs121909208
rs121909208
0.724 0.240 5 136056780 missense variant C/T snv 7.0E-06
CUI: C4700127
Disease: Thiel-behnke
Thiel-behnke
0.010 1.000 1 2007 2007