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: rs12721054
rs12721054
3 19 44919330 3 prime UTR variant A/G snv 3.7E-02 0.800 1.000 6 2012 2019
dbSNP: rs4420638
rs4420638
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 5 2007 2018
dbSNP: rs438811
rs438811
5 19 44913484 non coding transcript exon variant C/T snv 0.29 0.700 1.000 2 2015 2018
dbSNP: rs12721046
rs12721046
8 19 44917997 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs390082
rs390082
1 19 44913574 non coding transcript exon variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs483082
rs483082
4 1.000 0.080 19 44912921 non coding transcript exon variant G/T snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs56131196
rs56131196
6 0.925 0.160 19 44919589 downstream gene variant G/A snv 0.18 0.700 1.000 1 2018 2018