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: rs17080102
rs17080102
3 6 150683634 5 prime UTR variant G/C snv 8.6E-02 0.700 1.000 6 2013 2019
dbSNP: rs113397083
rs113397083
1 6 150663605 non coding transcript exon variant G/A snv 8.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs17080093
rs17080093
2 6 150676304 intron variant C/T snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs62434109
rs62434109
5 6 150654176 intron variant T/G snv 8.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs62434120
rs62434120
3 6 150671234 intron variant T/A snv 9.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs62434129
rs62434129
6 6 150687701 intron variant A/G;T snv 8.8E-02 0.700 1.000 1 2018 2018