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: rs1057519583
rs1057519583
STN1
3 0.882 0.160 10 103900115 missense variant C/G snv 0.800 0
dbSNP: rs765462548
rs765462548
STN1
3 0.882 0.160 10 103898989 missense variant C/A;T snv 4.0E-06; 2.4E-05 0.800 0