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: rs60005721
rs60005721
CMAHP ; LOC101928663
1 1.000 0.040 6 25262991 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs62392365
rs62392365
CMAHP ; CARMIL1
2 1.000 0.040 6 25371141 intron variant A/T snv 3.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs6918354
rs6918354
CMAHP ; CARMIL1
1 1.000 0.040 6 25444386 intron variant A/T snv 0.79 0.700 1.000 1 2019 2019
dbSNP: rs6942227
rs6942227
CMAHP
2 0.925 0.040 6 25177280 intron variant A/G snv 9.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs73388146
rs73388146
CMAHP
1 1.000 0.040 6 25170440 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs7752195
rs7752195
CMAHP ; CARMIL1
2 1.000 0.040 6 25418866 intron variant T/C snv 0.93 0.700 1.000 1 2017 2017
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