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: rs16937956
rs16937956
2 11 8382954 regulatory region variant A/G snv 0.35 0.700 1.000 2 2017 2018
dbSNP: rs10769908
rs10769908
4 11 8462542 intron variant C/T snv 0.55 0.700 1.000 1 2009 2009
dbSNP: rs10840060
rs10840060
1 11 8478498 intron variant A/C snv 0.45 0.700 1.000 1 2015 2015
dbSNP: rs4929949
rs4929949
4 1.000 0.080 11 8583046 intron variant T/C snv 0.46 0.700 1.000 1 2010 2010