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: rs6899676
rs6899676
2 6 10895027 intron variant A/G snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs9393800
rs9393800
3 6 10951504 intron variant A/G snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs2153157
rs2153157
1 6 10897255 intron variant G/A snv 0.55 0.800 1.000 2 2009 2012
dbSNP: rs9358956
rs9358956
1 6 10887020 5 prime UTR variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12211124
rs12211124
1 6 10886352 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018