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: rs7708584
rs7708584
3 5 154163906 intron variant A/G snv 0.58 0.700 1.000 2 2013 2017
dbSNP: rs7715256
rs7715256
1 5 154158333 non coding transcript exon variant G/T snv 0.55 0.700 1.000 2 2015 2016
dbSNP: rs815610
rs815610
1 5 154137618 intron variant C/G snv 0.47 0.700 1.000 2 2015 2018
dbSNP: rs10044136
rs10044136
1 5 154167248 intron variant G/C snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs1428121
rs1428121
1 5 154167935 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs4958702
rs4958702
1 5 154164952 intron variant T/C snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs7701886
rs7701886
2 5 154167849 intron variant G/A snv 0.49 0.700 1.000 1 2019 2019