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: rs10811625
rs10811625
1 1.000 0.040 9 21826841 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10965144
rs10965144
1 1.000 0.040 9 21808914 5 prime UTR variant C/T snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs3900787
rs3900787
1 1.000 0.040 9 21828111 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs3922992
rs3922992
1 1.000 0.040 9 21827407 intron variant A/G snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs3927737
rs3927737
1 1.000 0.040 9 21827993 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs7023954
rs7023954
2 0.925 0.040 9 21816759 missense variant G/A snv 0.40 0.42 0.700 1.000 1 2009 2009
dbSNP: rs7027989
rs7027989
2 0.925 0.120 9 21817755 intron variant A/G;T snv 0.700 1.000 1 2009 2009