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: rs1537370
rs1537370
1 1.000 9 22084311 intron variant C/T snv 0.55 0.800 1.000 3 2011 2013
dbSNP: rs10511701
rs10511701
2 9 22112600 intron variant T/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs1333043
rs1333043
2 9 22106732 intron variant T/A snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs1537371
rs1537371
1 9 22099569 intron variant C/A;T snv 0.700 1.000 2 2011 2013
dbSNP: rs1556516
rs1556516
1 9 22100177 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs7341786
rs7341786
2 9 22112242 intron variant A/C snv 0.65 0.700 1.000 2 2011 2013
dbSNP: rs1333050
rs1333050
1 9 22125914 intron variant C/T snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs188234402
rs188234402
1 9 22029058 intron variant T/A snv 2.1E-05 0.700 1.000 1 2013 2013
dbSNP: rs201049435
rs201049435
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 6.9E-03 0.700 1.000 1 2013 2013
dbSNP: rs34059530
rs34059530
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 0.700 1.000 1 2013 2013
dbSNP: rs397733626
rs397733626
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 0.58 0.700 1.000 1 2013 2013
dbSNP: rs4451405
rs4451405
1 9 22071751 intron variant C/T snv 0.69 0.700 1.000 1 2013 2013
dbSNP: rs565448157
rs565448157
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 8.0E-04 0.700 1.000 1 2013 2013
dbSNP: rs7341791
rs7341791
1 9 22112428 intron variant A/G snv 0.65 0.700 1.000 1 2013 2013
dbSNP: rs7857118
rs7857118
1 9 22124141 intron variant A/T snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs7859362
rs7859362
2 9 22105928 intron variant T/C snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs1004638
rs1004638
2 1.000 0.040 9 22115590 intron variant A/C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10738609
rs10738609
3 1.000 0.040 9 22114496 intron variant A/C;G;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10757269
rs10757269
3 1.000 0.040 9 22072265 intron variant A/C;G snv 0.700 1.000 2 2011 2013
dbSNP: rs10811647
rs10811647
3 1.000 0.040 9 22065003 intron variant C/G;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10811651
rs10811651
2 1.000 0.040 9 22067831 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs10965224
rs10965224
2 1.000 0.040 9 22067277 intron variant T/A snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs1333039
rs1333039
2 1.000 0.040 9 22065658 splice region variant G/A;C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs1537374
rs1537374
2 1.000 0.040 9 22116047 intron variant A/G snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs1556515
rs1556515
2 1.000 0.040 9 22036368 non coding transcript exon variant C/T snv 0.71 0.700 1.000 2 2011 2013