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: rs1135205
rs1135205
1 6 134960657 3 prime UTR variant C/T snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs7739722
rs7739722
1 6 134961087 3 prime UTR variant T/C snv 0.35 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: rs9389248
rs9389248
2 6 134961518 3 prime UTR variant T/C snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs13196486
rs13196486
1 6 134962736 3 prime UTR variant C/G snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs9399129
rs9399129
1 6 134964010 3 prime UTR variant C/A snv 0.49 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: rs13199205
rs13199205
1 6 134965367 intron variant T/A;C;G 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: rs4895434
rs4895434
1 6 134972227 intron variant G/A snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs4896119
rs4896119
1 6 134972253 intron variant C/T snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs4895435
rs4895435
1 6 134972325 intron variant C/A snv 0.62 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: rs7755680
rs7755680
1 6 134973121 intron variant A/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs4895436
rs4895436
1 6 134973863 intron variant G/A snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs9376075
rs9376075
1 6 134975825 intron variant A/G snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs10484496
rs10484496
1 6 134978544 intron variant T/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs13214669
rs13214669
1 6 134978821 intron variant T/C snv 0.33 0.31 0.700 1.000 1 2012 2012
dbSNP: rs11754021
rs11754021
1 6 134987237 intron variant A/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs13218642
rs13218642
1 6 134988802 intron variant A/G snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs4451151
rs4451151
1 6 134989408 intron variant C/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs13197750
rs13197750
1 6 134991242 intron variant G/A snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs6902954
rs6902954
1 6 134992856 intron variant C/A snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs7761964
rs7761964
1 6 134993127 intron variant T/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs6909975
rs6909975
1 6 134994432 intron variant C/T snv 0.59 0.700 1.000 1 2012 2012