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: rs16917546
rs16917546
6 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs10995240
rs10995240
2 10 62628871 intron variant G/C snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs12413946
rs12413946
2 10 62671446 non coding transcript exon variant T/C snv 6.2E-02 0.700 1.000 1 2016 2016