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: rs3867595
rs3867595
1 17 7476457 intron variant G/C snv 1.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs67462449
rs67462449
1 17 7474221 intron variant TTT/-;T;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT delins 0.700 1.000 1 2019 2019