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: rs36027220
rs36027220
1.000 13 37009283 missense variant G/C snv 3.9E-03 4.0E-03
CUI: C4015160
Disease: PONTOCEREBELLAR HYPOPLASIA, TYPE 1C
PONTOCEREBELLAR HYPOPLASIA, TYPE 1C
0.800 1.000 1 2014 2014
dbSNP: rs606231285
rs606231285
1.000 13 37000810 missense variant C/G;T snv
CUI: C4015160
Disease: PONTOCEREBELLAR HYPOPLASIA, TYPE 1C
PONTOCEREBELLAR HYPOPLASIA, TYPE 1C
0.800 0