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: rs34156328
rs34156328
2 10 45507812 intron variant AAA/-;AA;AAAA;AAAAA delins 0.700 1.000 2 2016 2017
dbSNP: rs11239541
rs11239541
3 10 45506418 intron variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs149604913
rs149604913
2 10 45499558 intron variant T/C snv 1.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs77677521
rs77677521
4 10 45457448 3 prime UTR variant C/G snv 1.3E-02 0.700 1.000 1 2017 2017