Gene: CCN4 ×
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: rs2977536
rs2977536
CCN4
4 0.851 0.080 8 133207034 intron variant G/C snv 0.36 0.020 1.000 2 2014 2015
dbSNP: rs11778573
rs11778573
CCN4
4 0.851 0.080 8 133216687 intron variant T/G snv 0.59 0.010 1.000 1 2015 2015
dbSNP: rs16893344
rs16893344
CCN4
7 0.807 0.160 8 133194036 intron variant C/T snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs2929970
rs2929970
CCN4
5 0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 0.010 1.000 1 2014 2014
dbSNP: rs2929973
rs2929973
CCN4
5 0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 0.010 1.000 1 2014 2014
dbSNP: rs2977549
rs2977549
CCN4
3 0.882 0.080 8 133229790 3 prime UTR variant C/A;T snv 0.010 1.000 1 2015 2015
dbSNP: rs3739262
rs3739262
CCN4
3 0.882 0.080 8 133193470 intron variant G/A snv 0.24 0.010 1.000 1 2014 2014
dbSNP: rs62514004
rs62514004
CCN4
8 0.790 0.240 8 133190246 upstream gene variant A/G snv 0.28 0.010 1.000 1 2015 2015
dbSNP: rs754958
rs754958
CCN4
3 0.882 0.080 8 133226528 intron variant G/A;T snv 0.010 1.000 1 2014 2014