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: rs11265142
rs11265142
1 1 159130118 intron variant A/G snv 8.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs2518569
rs2518569
1 1 159125785 intron variant T/G snv 0.80 0.700 1.000 1 2012 2012