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: rs2279463
rs2279463
4 1.000 0.080 6 160247357 intron variant A/G;T snv 0.700 1.000 2 2010 2012
dbSNP: rs316029
rs316029
1 6 160265636 intron variant T/C snv 0.89 0.700 1.000 1 2011 2011