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: rs11984041
rs11984041
3 0.925 0.080 7 18992312 intron variant C/T snv 0.13 0.830 1.000 3 2012 2015
dbSNP: rs17347800
rs17347800
1 7 18477656 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs2389995
rs2389995
3 0.925 0.200 7 18933395 intron variant A/G snv 6.0E-02 0.020 1.000 2 2013 2017
dbSNP: rs28688791
rs28688791
1 7 18999982 3 prime UTR variant T/A;C snv 0.020 1.000 2 2018 2019
dbSNP: rs2074633
rs2074633
2 7 18996297 3 prime UTR variant T/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs2240419
rs2240419
3 0.925 0.200 7 18935566 intron variant T/A;C snv 0.010 1.000 1 2013 2013