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: rs11085824
rs11085824
4 19 12890733 upstream gene variant A/G snv 0.31 0.800 1.000 2 2009 2017
dbSNP: rs11085825
rs11085825
3 19 12896644 intron variant C/T snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs56397034
rs56397034
3 19 12889736 upstream gene variant G/C snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs741702
rs741702
3 19 12913436 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs8012
rs8012
2 19 12899706 3 prime UTR variant A/G snv 0.61 0.64 0.700 1.000 1 2016 2016