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: rs62638745
rs62638745
3 0.878 0.071 19 11378051 missense variant T/C snp 6.3E-03 7.1E-03 0.700 0
dbSNP: rs80358193
rs80358193
2 0.923 0.036 1 231374041 missense variant G/C snp 0.020 1.000 2 2008 2008
dbSNP: rs137853036
rs137853036
2 0.923 0.036 2 46380281 missense variant G/A,T snp 0.010 1.000 1 2014 2014
dbSNP: rs182123615
rs182123615
4 0.878 0.143 9 5070058 splice region variant T/C snp 3.6E-04 6.7E-04 0.010 1.000 1 2017 2017
dbSNP: rs77375493
rs77375493
106 0.504 0.536 9 5073770 missense variant G/A,T snp 3.5E-04 2.9E-04 0.010 1.000 1 2008 2008