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: rs4506565
rs4506565
18 0.790 0.280 10 112996282 intron variant A/G;T snv 0.800 1.000 3 2010 2019
dbSNP: rs7903146
rs7903146
16 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 2 2009 2019
dbSNP: rs12243326
rs12243326
3 0.925 0.160 10 113029056 intron variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs17747324
rs17747324
3 0.925 0.160 10 112992744 intron variant T/C snv 0.17 0.700 1.000 1 2019 2019