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: rs1373855924
rs1373855924
VPS33B ; LOC105370970
4 0.851 0.240 15 91009812 missense variant C/T snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs780274878
rs780274878
DSP
1 1.000 0.040 6 7583428 missense variant G/C snv 4.0E-06 0.010 1.000 1 2010 2010