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: rs7768330
rs7768330
1 6 151981077 intron variant A/G snv 5.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs9340922
rs9340922
1 6 151971471 intron variant A/C snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs9340996
rs9340996
1 6 152021653 intron variant G/T snv 1.1E-03 0.700 1.000 1 2012 2012
dbSNP: rs9341023
rs9341023
6 6 152062578 intron variant C/T snv 0.700 1.000 1 2012 2012
dbSNP: rs9341074
rs9341074
1 6 152101320 3 prime UTR variant T/A snv 1.3E-02 0.700 1.000 1 2012 2012