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: rs11572325
rs11572325
3 0.925 0.080 1 59896030 intron variant A/T snv 0.12 0.010 1.000 1 2019 2019
dbSNP: rs2280275
rs2280275
3 0.925 0.040 1 59901568 intron variant T/C snv 0.23 0.010 1.000 1 2019 2019
dbSNP: rs890293
rs890293
4 0.851 0.200 1 59926822 upstream gene variant C/A snv 8.6E-02 0.010 1.000 1 2019 2019