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: rs1046411
rs1046411
CNNM2
1 10 103078059 3 prime UTR variant G/A snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs12783467
rs12783467
CNNM2
1 10 102948555 intron variant A/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs200510190
rs200510190
CNNM2
2 10 103031838 intron variant C/- del 0.41 0.700 1.000 1 2016 2016