Source: BEFREE ×
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: rs150594290
rs150594290
3 1.000 0.080 1 21575894 missense variant G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs373345919
rs373345919
5 0.882 0.080 17 42909364 stop gained C/T snv 2.8E-05 2.8E-05 0.010 1.000 1 2000 2000
dbSNP: rs786204473
rs786204473
2 0.925 0.080 1 21573673 missense variant G/A snv 0.010 1.000 1 2002 2002