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: rs10445033
rs10445033
1 16 88774054 intron variant G/A snv 0.49 0.800 1.000 2 2012 2019
dbSNP: rs2608604
rs2608604
1 16 88783013 intron variant A/G;T snv 0.800 1.000 2 2012 2017
dbSNP: rs202099525
rs202099525
1 16 88721629 missense variant G/A snv 4.4E-04 4.7E-04 0.700 1.000 1 2016 2016
dbSNP: rs2932690
rs2932690
1 16 88776545 intron variant G/A snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs4238686
rs4238686
2 16 88722526 non coding transcript exon variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs475596
rs475596
1 16 88780543 intron variant G/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs750739
rs750739
1 16 88741200 non coding transcript exon variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs889761
rs889761
1 16 88775807 intron variant G/C snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs9932423
rs9932423
1 16 88780441 intron variant C/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs9933309
rs9933309
1 16 88778524 intron variant T/C snv 0.72 0.700 1.000 1 2012 2012