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: rs10128711
rs10128711
2 11 18611437 intron variant T/C snv 0.64 0.55 0.700 1.000 1 2018 2018
dbSNP: rs10832961
rs10832961
2 11 18632410 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11024735
rs11024735
2 11 18617620 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11024739
rs11024739
3 11 18624296 intron variant C/A;G snv 0.700 1.000 1 2012 2012