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: rs267607033
rs267607033
SEMA4A
2 0.925 0.080 1 156162993 missense variant G/C snv 1.4E-05 0.800 1.000 2 2006 2012
dbSNP: rs267607034
rs267607034
SEMA4A
3 0.882 0.080 1 156163009 missense variant T/G snv 0.800 1.000 2 2006 2012