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: rs11209026
rs11209026
5 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.900 1.000 3 2007 2020
dbSNP: rs10889677
rs10889677
2 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.820 1.000 1 2009 2020
dbSNP: rs2201841
rs2201841
4 0.716 0.440 1 67228519 intron variant A/G;T snv 0.820 1.000 1 2010 2017