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: rs183241934
rs183241934
2 1.000 4 53140760 intron variant A/C snv 5.0E-04 0.700 1.000 1 2018 2018
dbSNP: rs188539274
rs188539274
2 1.000 4 52893799 intron variant C/T snv 1.4E-03 0.700 1.000 1 2018 2018
dbSNP: rs765333492
rs765333492
2 1.000 4 53021103 intron variant T/C snv 0.700 1.000 1 2018 2018