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: rs3024971
rs3024971
7 0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs324011
rs324011
12 0.742 0.360 12 57108399 intron variant C/T snv 0.32 0.020 1.000 2 2013 2015
dbSNP: rs1059513
rs1059513
11 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 0.010 1.000 1 2013 2013
dbSNP: rs167769
rs167769
5 0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 0.010 1.000 1 2015 2015