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: rs77204473
rs77204473
2 11 116934348 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs78692246
rs78692246
2 11 116920591 intron variant G/A snv 7.3E-02 0.700 1.000 1 2019 2019