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: rs10936602
rs10936602
3 0.882 0.240 3 169818849 upstream gene variant T/C snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs10936603
rs10936603
1 1.000 0.160 3 169827864 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1920119
rs1920119
1 1.000 0.160 3 169822609 synonymous variant T/C snv 0.50 0.50 0.700 1.000 1 2013 2013
dbSNP: rs9833035
rs9833035
1 1.000 0.160 3 169835710 intron variant G/T snv 0.30 0.700 1.000 1 2013 2013