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: rs10872678
rs10872678
1 6 151718829 intron variant T/C snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs1101081
rs1101081
1 6 151711782 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs7772579
rs7772579
1 6 151721367 intron variant A/C snv 0.32 0.700 1.000 1 2019 2019