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: rs10047459
rs10047459
1 11 116851110 intron variant C/T snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs10047462
rs10047462
3 11 116851325 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12099358
rs12099358
2 11 116855332 non coding transcript exon variant C/A snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs5072
rs5072
5 11 116836867 intron variant A/G snv 0.89 0.700 1.000 1 2012 2012
dbSNP: rs689243
rs689243
2 11 116851977 intron variant G/C snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs888245
rs888245
1 11 116853021 intron variant C/G snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs888246
rs888246
1 11 116853516 intron variant C/T snv 8.6E-02 0.700 1.000 1 2012 2012