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: rs765431049
rs765431049
GNGT1 ; TFPI2 ; LOC105375401
4 0.925 0.040 7 93890271 missense variant C/T snv 1.6E-05 0.010 1.000 1 2004 2004