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: rs3131009
rs3131009
5 0.925 0.080 6 31131055 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs3132545
rs3132545
4 1.000 6 31121348 intron variant A/G snv 0.76 0.700 1.000 1 2010 2010
dbSNP: rs3132546
rs3132546
4 1.000 6 31120802 intron variant A/G snv 0.78 0.700 1.000 1 2010 2010
dbSNP: rs3132551
rs3132551
4 1.000 6 31118105 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs3132552
rs3132552
4 1.000 6 31117492 synonymous variant A/G snv 0.76 0.78 0.700 1.000 1 2010 2010
dbSNP: rs3132553
rs3132553
4 1.000 6 31117423 synonymous variant A/G snv 0.75 0.78 0.700 1.000 1 2010 2010
dbSNP: rs3778639
rs3778639
4 1.000 6 31125999 intron variant A/C;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs3823417
rs3823417
4 1.000 6 31133092 intron variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs3823418
rs3823418
8 0.925 0.120 6 31133165 intron variant G/A snv 0.23 0.700 1.000 1 2009 2009
dbSNP: rs386580036
rs386580036
4 1.000 6 31117492 synonymous variant A/G snv 0.700 1.000 1 2010 2010
dbSNP: rs386580037
rs386580037
4 1.000 6 31117423 synonymous variant A/G snv 0.700 1.000 1 2010 2010
dbSNP: rs4294047
rs4294047
4 1.000 6 31133806 intron variant G/A snv 8.9E-02 0.700 1.000 1 2010 2010
dbSNP: rs527476195
rs527476195
6 0.925 0.120 6 31133165 intron variant G/A snv 0.700 1.000 1 2009 2009
dbSNP: rs528878831
rs528878831
5 0.925 0.080 6 31131055 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs540151006
rs540151006
4 1.000 6 31120802 intron variant A/G snv 0.700 1.000 1 2010 2010
dbSNP: rs540385376
rs540385376
5 0.925 0.120 6 31117605 non coding transcript exon variant C/A snv 0.700 1.000 1 2010 2010
dbSNP: rs541134362
rs541134362
4 1.000 6 31118905 intron variant C/T snv 0.700 1.000 1 2010 2010
dbSNP: rs542420252
rs542420252
4 1.000 6 31133806 intron variant G/A snv 0.700 1.000 1 2010 2010
dbSNP: rs545914110
rs545914110
4 1.000 6 31124215 intron variant A/G snv 0.700 1.000 1 2009 2009
dbSNP: rs546583999
rs546583999
4 1.000 6 31118105 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs553317370
rs553317370
4 1.000 6 31121348 intron variant A/G snv 0.700 1.000 1 2010 2010
dbSNP: rs555542204
rs555542204
4 1.000 6 31118625 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs559951725
rs559951725
4 1.000 6 31133092 intron variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs560839399
rs560839399
4 1.000 6 31124085 intron variant A/G snv 0.700 1.000 1 2009 2009
dbSNP: rs573422310
rs573422310
4 1.000 6 31121079 intron variant T/C snv 0.700 1.000 1 2010 2010