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: rs67162484
rs67162484
1 22 42719514 intron variant TTCT/-;TTCTTTCT delins 0.41 0.700 1.000 1 2018 2018