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: rs201631095
rs201631095
2 1.000 0.080 19 8208084 intron variant AAA/-;A;AA;AAAA;AAAAA;AAAAAA delins 0.700 1.000 1 2018 2018
dbSNP: rs7253584
rs7253584
2 1.000 0.080 19 8222034 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs7259572
rs7259572
2 1.000 0.080 19 8226788 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs9749262
rs9749262
2 1.000 0.080 19 8223873 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018