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: rs11741861
rs11741861
3 0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02 0.800 1.000 2 2012 2017
dbSNP: rs10065172
rs10065172
8 0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 0.010 1.000 1 2011 2011
dbSNP: rs4958847
rs4958847
8 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.010 1.000 1 2008 2008