Gene: CNNM2 ×
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: rs11191548
rs11191548
CNNM2
10 0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 0.700 1.000 8 2009 2018
dbSNP: rs140473396
rs140473396
CNNM2
1 10 103036129 intron variant ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC delins 0.700 1.000 1 2019 2019
dbSNP: rs943037
rs943037
CNNM2
2 10 103076162 synonymous variant C/T snv 0.12 8.3E-02 0.700 1.000 1 2016 2016