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: rs370229832
rs370229832
F2
2 0.925 0.080 11 46739293 missense variant T/C snv 3.2E-05 6.3E-05 0.010 1.000 1 2007 2007