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: rs62392365
rs62392365
CMAHP ; CARMIL1
2 1.000 0.040 6 25371141 intron variant A/T snv 3.2E-02 0.700 1.000 2 2018 2019
dbSNP: rs116418977
rs116418977
CMAHP ; CARMIL1
1 6 25365660 intron variant C/T snv 4.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs77482156
rs77482156
CMAHP
1 6 25199625 intron variant T/C snv 3.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs7774567
rs7774567
CMAHP ; CARMIL1
2 1.000 0.040 6 25425298 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs79738691
rs79738691
CMAHP
1 6 25148332 intron variant A/G snv 7.7E-02 0.700 1.000 1 2018 2018