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: rs2291909
rs2291909
2 12 117247112 intron variant T/G snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs7960451
rs7960451
2 12 117235437 intron variant C/T snv 8.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs9658292
rs9658292
5 12 117318980 intron variant G/C snv 9.4E-04 0.700 1.000 1 2012 2012
dbSNP: rs9658449
rs9658449
2 12 117252327 intron variant A/G snv 3.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs9658465
rs9658465
3 12 117247093 intron variant T/G snv 2.3E-02 0.700 1.000 1 2012 2012