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: rs11220462
rs11220462
3 11 126374057 intron variant G/A snv 0.12 0.800 1.000 4 2010 2019
dbSNP: rs11220463
rs11220463
3 11 126378316 intron variant A/T snv 0.12 0.700 1.000 2 2016 2018
dbSNP: rs4307732
rs4307732
2 11 126375060 non coding transcript exon variant G/A snv 0.13 0.700 1.000 2 2015 2018
dbSNP: rs76970536
rs76970536
3 11 126380785 intron variant G/A;T snv 0.700 1.000 2 2019 2019
dbSNP: rs10893499
rs10893499
2 11 126372084 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs59379014
rs59379014
2 11 126358105 intron variant C/T snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs68055275
rs68055275
3 11 126369248 intron variant -/T;TT delins 0.700 1.000 1 2018 2018