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: rs12634907
rs12634907
2 3 158509097 intron variant A/G snv 0.28 0.700 1.000 2 2019 2019
dbSNP: rs1595029
rs1595029
2 3 158523978 intron variant A/C snv 0.52 0.700 1.000 1 2017 2017