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: rs11014166
rs11014166
10 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 2 2009 2017
dbSNP: rs1813353
rs1813353
5 10 18418519 intron variant T/C snv 0.29 0.700 1.000 2 2017 2018
dbSNP: rs11014267
rs11014267
2 10 18448045 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12243859
rs12243859
2 10 18451703 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs67744136
rs67744136
2 10 18416407 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018