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: rs16921914
rs16921914
1 11 31189224 intron variant G/A snv 0.22 0.800 1.000 1 2009 2009
dbSNP: rs163879
rs163879
2 11 30930127 intron variant C/T snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs273573
rs273573
1 11 30889444 intron variant A/C snv 0.69 0.700 1.000 1 2018 2018