Gene: CMAHP ×
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: rs17251430
rs17251430
CMAHP ; CARMIL1
2 6 25397775 intron variant A/G snv 5.3E-02 0.700 1.000 1 2009 2009
dbSNP: rs17316893
rs17316893
CMAHP ; CARMIL1
2 6 25394211 intron variant C/T snv 5.3E-02 0.700 1.000 1 2009 2009
dbSNP: rs723048
rs723048
CMAHP ; LOC105375106
1 6 25273938 intron variant G/A snv 0.82 0.700 1.000 1 2019 2019
dbSNP: rs9467477
rs9467477
CMAHP ; CARMIL1
2 6 25369838 intron variant T/A snv 9.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs985984
rs985984
CMAHP ; CARMIL1
2 6 25401951 intron variant C/G;T snv 0.700 1.000 1 2009 2009