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: rs155524
rs155524
1 3 37520650 intron variant G/A snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs174829
rs174829
1 3 37494086 intron variant A/G snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs2507948
rs2507948
1 3 37790681 intron variant A/G snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs267519
rs267519
1 3 37495221 intron variant A/G snv 0.74 0.700 1.000 1 2019 2019