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: rs9268856
rs9268856
4 0.807 0.240 6 32461942 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9268862
rs9268862
2 0.925 0.160 6 32462390 intron variant A/C snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs9268895
rs9268895
1 1.000 0.040 6 32464185 intron variant A/G snv 0.29 0.700 1.000 1 2013 2013