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: rs610604
rs610604
5 0.827 0.240 6 137878280 intron variant G/T snv 0.58 0.860 1.000 10 2009 2015
dbSNP: rs582757
rs582757
8 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.800 1.000 3 2012 2016
dbSNP: rs643177
rs643177
1 1.000 0.040 6 137874556 intron variant T/C snv 0.70 0.700 1.000 2 2015 2015
dbSNP: rs2230926
rs2230926
27 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 0.020 1.000 2 2011 2012