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: rs7801581
rs7801581
5 7 27184152 intron variant C/T snv 0.24 0.700 1.000 2 2015 2018
dbSNP: rs4722669
rs4722669
1 7 27187169 intron variant C/G;T snv 5.7E-02 0.700 1.000 1 2019 2019