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: rs2857461
rs2857461
3 0.882 0.160 22 29272015 intron variant C/T snv 0.98 0.010 1.000 1 2012 2012
dbSNP: rs4820804
rs4820804
1 1.000 0.040 22 29273704 intron variant T/C snv 0.40 0.35 0.010 1.000 1 2012 2012