Gene: INF2 ×
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: rs387907037
rs387907037
INF2
2 1.000 14 104701748 missense variant T/C snv 0.010 1.000 1 2013 2013