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: rs121909295
rs121909295
SGCD
2 0.925 0.200 5 156595042 stop gained C/G;T snv 4.1E-06; 8.1E-06 0.700 1.000 2 1997 2009
dbSNP: rs1175344271
rs1175344271
SGCD
2 0.925 0.200 5 156757668 stop gained C/A snv 0.700 1.000 1 2006 2006
dbSNP: rs121909298
rs121909298
SGCD
4 0.925 0.040 5 156595000 missense variant T/G snv 2.0E-04 1.3E-04 0.700 1.000 1 2000 2000
dbSNP: rs1267810339
rs1267810339
SGCD
2 0.925 0.200 5 156344678 splice donor variant G/A snv 4.3E-06 0.700 0
dbSNP: rs1554137109
rs1554137109
SGCD
2 0.925 0.200 5 156757620 frameshift variant A/- delins 0.700 0
dbSNP: rs1554137130
rs1554137130
SGCD
2 0.925 0.200 5 156757705 splice donor variant G/T snv 0.700 0
dbSNP: rs397517923
rs397517923
SGCD
2 0.925 0.200 5 156344554 stop gained C/A;T snv 1.2E-04 6.3E-05 0.700 0
dbSNP: rs727503422
rs727503422
SGCD
3 0.925 0.200 5 156508703 splice donor variant G/A snv 0.700 0