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: rs1533326
rs1533326
1 1.000 0.040 15 90211722 intron variant A/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs34560261
rs34560261
3 0.882 0.040 15 90191194 intron variant C/T snv 0.12 0.700 1.000 1 2018 2018