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: rs10254101
rs10254101
3 7 151718450 intron variant C/T snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs6464165
rs6464165
2 7 151716038 intron variant T/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs7805747
rs7805747
5 1.000 0.080 7 151710715 intron variant G/A snv 0.26 0.700 1.000 1 2016 2016