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: rs150109621
rs150109621
3 1.000 0.040 22 46429532 intron variant C/T snv 5.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs150381023
rs150381023
3 1.000 0.040 22 46423108 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs535263906
rs535263906
3 1.000 0.040 22 46422493 intron variant G/A snv 8.6E-03 0.700 1.000 1 2019 2019