Gene: CADM2 ×
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: rs13078960
rs13078960
CADM2
2 3 85758440 intron variant T/G snv 0.15 0.700 1.000 3 2015 2018
dbSNP: rs12495178
rs12495178
CADM2
2 3 85836927 intron variant T/A;C snv 0.700 1.000 2 2017 2019
dbSNP: rs9818122
rs9818122
CADM2 ; CADM2-AS2
2 3 85811914 intron variant T/C snv 0.20 0.700 1.000 2 2017 2019
dbSNP: rs13068138
rs13068138
CADM2
1 3 85760275 intron variant C/T snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs13078807
rs13078807
CADM2
5 0.925 0.120 3 85835000 intron variant A/G snv 0.15 0.700 1.000 1 2010 2010
dbSNP: rs13098327
rs13098327
CADM2
2 3 85771031 intron variant G/A snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs62261676
rs62261676
CADM2
1 3 85649427 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs6762267
rs6762267
CADM2
1 3 85463965 intron variant C/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs7630382
rs7630382
CADM2 ; SNORA95
1 3 85061957 intron variant C/T snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs9813495
rs9813495
CADM2
4 3 85777231 intron variant A/G snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs9852127
rs9852127
CADM2
2 3 85777586 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs9852859
rs9852859
CADM2
2 3 85793191 intron variant T/C snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs9866543
rs9866543
CADM2
1 3 85931931 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs9876664
rs9876664
CADM2
1 3 85757163 intron variant G/T snv 0.40 0.700 1.000 1 2019 2019