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: rs10872427
rs10872427
1 6 135032314 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs11752907
rs11752907
1 6 135070357 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11757577
rs11757577
2 6 135070327 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12663810
rs12663810
1 6 134968644 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs13199205
rs13199205
1 6 134965367 intron variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs13209780
rs13209780
1 6 135023657 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4594969
rs4594969
1 6 134964448 3 prime UTR variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4895439
rs4895439
1 6 134997716 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4896120
rs4896120
1 6 134972374 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4896130
rs4896130
1 6 135033980 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs566152659
rs566152659
1 6 134961088 3 prime UTR variant GCT/- delins 0.700 1.000 1 2012 2012
dbSNP: rs6923765
rs6923765
1 6 135014038 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7743042
rs7743042
1 6 135098696 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7745098
rs7745098
2 1.000 0.120 6 135093866 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7750300
rs7750300
1 6 135029812 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7750574
rs7750574
1 6 135029794 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs9373122
rs9373122
1 6 135052396 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9376082
rs9376082
1 6 135025251 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs9389261
rs9389261
1 6 135050010 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9389264
rs9389264
1 6 135079974 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs9402677
rs9402677
1 6 135049570 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9483783
rs9483783
2 6 135079902 intron variant T/C snv 2.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs13192235
rs13192235
2 6 135025213 intron variant G/A snv 4.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs7775698
rs7775698
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 3 2010 2012
dbSNP: rs9376084
rs9376084
1 6 135038908 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012