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: rs10766309
rs10766309
2 11 16235171 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11023906
rs11023906
3 11 16302860 intron variant G/A snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs12799126
rs12799126
3 11 16286917 intron variant G/T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs2218001
rs2218001
2 11 16320669 intron variant A/C;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7118275
rs7118275
2 11 16250132 intron variant C/T snv 0.78 0.700 1.000 1 2018 2018
dbSNP: rs893311
rs893311
2 11 16296972 intron variant G/T snv 0.16 0.700 1.000 1 2018 2018