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: rs3094212
rs3094212
5 1.000 6 31117993 non coding transcript exon variant G/A snv 0.58 0.700 1.000 2 2009 2010
dbSNP: rs3095320
rs3095320
4 1.000 6 31120157 intron variant G/A;C snv 0.700 1.000 2 2009 2010
dbSNP: rs551894425
rs551894425
4 1.000 6 31117993 non coding transcript exon variant G/A snv 0.700 1.000 2 2009 2010
dbSNP: rs562436976
rs562436976
4 1.000 6 31120157 intron variant G/A;C snv 0.700 1.000 2 2009 2010
dbSNP: rs1042126
rs1042126
4 1.000 6 31116511 synonymous variant T/C snv 0.57 0.58 0.700 1.000 1 2010 2010
dbSNP: rs1042134
rs1042134
4 1.000 6 31115887 3 prime UTR variant G/A snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs1042147
rs1042147
4 1.000 6 31115379 3 prime UTR variant A/G snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs12207756
rs12207756
4 1.000 6 31118905 intron variant C/T snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs2239519
rs2239519
4 1.000 6 31121079 intron variant T/C snv 0.76 0.700 1.000 1 2010 2010
dbSNP: rs28732100
rs28732100
4 1.000 6 31136816 intron variant C/T snv 3.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs3094204
rs3094204
4 1.000 6 31124215 intron variant A/G snv 0.61 0.700 1.000 1 2009 2009
dbSNP: rs3094205
rs3094205
4 1.000 6 31124085 intron variant A/G snv 0.41 0.700 1.000 1 2009 2009
dbSNP: rs3094211
rs3094211
4 1.000 6 31118625 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs3094217
rs3094217
4 1.000 6 31115879 3 prime UTR variant G/A snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs3130560
rs3130560
4 1.000 6 31129676 intron variant T/A;G snv 8.2E-06; 0.74 0.700 1.000 1 2010 2010
dbSNP: rs3130982
rs3130982
4 1.000 6 31116298 synonymous variant G/C;T snv 0.56; 1.3E-02 0.700 1.000 1 2010 2010
dbSNP: rs3130984
rs3130984
4 1.000 6 31117187 missense variant T/C snv 0.76; 4.0E-06 0.78 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: rs386580036
rs386580036
4 1.000 6 31117492 synonymous variant A/G snv 0.700 1.000 1 2010 2010