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: rs113525195
rs113525195
2 14 23030112 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs8013143
rs8013143
4 14 23025068 intron variant A/G snv 0.43 0.700 1.000 1 2016 2016