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: rs4896120
rs4896120
1 6 134972374 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4896125
rs4896125
1 6 135021431 intron variant C/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs4896128
rs4896128
1 6 135028618 intron variant G/A snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs4896129
rs4896129
1 6 135028707 intron variant C/T snv 0.31 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: rs6569988
rs6569988
1 6 135031165 intron variant C/A snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs6569990
rs6569990
1 6 135044680 intron variant C/T snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs6902438
rs6902438
1 6 135015449 intron variant C/T snv 0.47 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: rs6904897
rs6904897
3 6 135061842 intron variant T/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs6908681
rs6908681
1 6 135016595 intron variant A/G snv 0.47 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
dbSNP: rs6913541
rs6913541
1 6 135087978 intron variant A/G snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs6914564
rs6914564
1 6 135082486 intron variant C/T snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs6915770
rs6915770
1 6 135048076 intron variant G/A snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs6919862
rs6919862
1 6 135031305 intron variant C/A snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs6923512
rs6923512
1 6 135014130 intron variant C/T snv 0.31 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: rs6923827
rs6923827
1 6 135014244 intron variant C/T snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs6929661
rs6929661
1 6 135007654 intron variant G/A snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs6940258
rs6940258
1 6 135044994 intron variant C/T snv 0.36 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: rs7742542
rs7742542
1 6 135037429 missense variant T/G snv 0.51 0.46 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