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: rs17367504
rs17367504
3 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 2 2011 2011
dbSNP: rs13306560
rs13306560
1 1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs1476413
rs1476413
1 0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 0.700 1.000 1 2011 2011
dbSNP: rs1801131
rs1801131
1 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.700 1.000 1 2011 2011
dbSNP: rs3818762
rs3818762
1 1 11790946 intron variant G/C snv 0.26; 1.7E-03 0.23 0.700 1.000 1 2011 2011
dbSNP: rs4846049
rs4846049
1 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs576853093
rs576853093
1 1 11790946 intron variant -/C;CACACACACACAC ins 6.2E-03 0.700 1.000 1 2011 2011