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: rs267607386
rs267607386
KRT12 ; LOC105371777
1 1.000 0.080 17 40863141 missense variant A/C snv 0.710 1.000 14 1997 2014