Gene: GCDH ×
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: rs121434368
rs121434368
GCDH ; SYCE2
2 0.925 0.120 19 12899471 missense variant C/T snv 0.010 1.000 1 2004 2004
dbSNP: rs1277384196
rs1277384196
GCDH ; SYCE2
2 0.925 0.120 19 12899507 missense variant T/C snv 4.0E-06 0.010 1.000 1 2004 2004