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: rs12721510
rs12721510
CRH
1 1.000 0.036 8 66178947 intergenic variant G/T snp 4.3E-02 0.700 2 1993 2006
dbSNP: rs72556399
rs72556399
CRH
1 1.000 0.036 8 66178643 5 prime UTR variant C/G snp 2.2E-04 0.700 2 1993 2006
dbSNP: rs74315291
rs74315291
2 0.923 0.036 1 154571682 missense variant G/A,C,T snp 0.030 1.000 3 2002 2013
dbSNP: rs773225799
rs773225799
1 1.000 0.036 20 63350471 missense variant T/C snp 1.2E-05 0.020 1.000 2 2002 2008
dbSNP: rs28931591
rs28931591
2 0.923 0.036 20 63350560 missense variant G/A snp 0.010 1.000 1 2003 2003
dbSNP: rs772253190
rs772253190
1 1.000 0.036 20 63350552 missense variant C/T snp 8.0E-06 0.010 1.000 1 2008 2008