Gene: MLIP ×
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: rs9296736
rs9296736
MLIP
1 6 54059899 intron variant T/C snv 0.51 0.800 1.000 1 2011 2011
dbSNP: rs9637973
rs9637973
MLIP
2 1.000 0.040 6 54038354 intron variant G/A snv 0.51 0.700 1.000 1 2018 2018