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: rs3810328
rs3810328
2 19 45864964 intron variant G/T snv 1.0E-01 0.700 1.000 1 2016 2016
dbSNP: rs62109854
rs62109854
1 19 45847117 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs76793172
rs76793172
1 19 45856536 intron variant C/T snv 7.9E-02 0.700 1.000 1 2016 2016