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: rs944002
rs944002
3 14 103106478 intron variant A/G snv 0.25 0.800 1.000 2 2011 2012
dbSNP: rs2274685
rs2274685
1 14 103108733 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7151779
rs7151779
1 14 103099825 upstream gene variant G/A snv 0.21 0.700 1.000 1 2019 2019