Gene: CARMIL1 ×
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: rs111722075
rs111722075
CMAHP ; CARMIL1
2 6 25373818 intron variant C/T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs202056061
rs202056061
CARMIL1
2 6 25494109 intron variant AGTT/- delins 2.8E-02 0.700 1.000 1 2017 2017