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
9 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 5 2009 2018
dbSNP: rs17037390
rs17037390
3 1.000 0.040 1 11800786 non coding transcript exon variant G/A snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs3753584
rs3753584
10 0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs6541006
rs6541006
2 1 11797469 intron variant A/G;T snv 0.700 1.000 1 2018 2018