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: rs2069443
rs2069443
2 1.000 0.080 7 151058086 intron variant T/G snv 0.32 0.010 1.000 1 2011 2011
dbSNP: rs2303933
rs2303933
1 1.000 0.080 7 151069712 intron variant A/C;G snv 0.010 1.000 1 2011 2011
dbSNP: rs2303937
rs2303937
1 1.000 0.080 7 151071699 synonymous variant G/A;C snv 0.48; 8.1E-06 0.010 1.000 1 2011 2011
dbSNP: rs2303941
rs2303941
1 1.000 0.080 7 151076200 non coding transcript exon variant T/C snv 3.0E-02 3.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs3793336
rs3793336
1 1.000 0.080 7 151065784 intron variant G/A;C snv 0.010 1.000 1 2009 2009