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: rs530424960
rs530424960
2 6 135028265 intron variant AAA/-;AA;AAAA;AAAAA delins 0.700 1.000 1 2016 2016
dbSNP: rs7775698
rs7775698
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs7776054
rs7776054
13 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs9399136
rs9399136
4 6 135081201 intron variant T/C snv 0.18 0.700 1.000 1 2019 2019