Source: ALL
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: rs11072766
rs11072766
IREB2
2 15 78479204 intron variant C/G;T snv 0.700 1.000 3 2010 2010
dbSNP: rs12910984
rs12910984
CHRNA3
8 0.827 0.080 15 78599285 intron variant G/A;C;T snv 0.700 1.000 3 2010 2010
dbSNP: rs12914385
rs12914385
CHRNA3
18 0.790 0.160 15 78606381 intron variant C/A;T snv 0.800 1.000 3 2010 2017
dbSNP: rs2568483
rs2568483
IREB2
2 15 78460001 intron variant G/A;T snv 0.700 1.000 3 2010 2010
dbSNP: rs2656069
rs2656069
IREB2
5 0.882 0.080 15 78453365 intron variant C/G;T snv 0.700 1.000 3 2010 2010
dbSNP: rs2656073
rs2656073
IREB2
2 15 78449934 intron variant T/A;G snv 0.700 1.000 3 2010 2010
dbSNP: rs2869032
rs2869032 		2 15 78422219 regulatory region variant C/G;T snv 0.700 1.000 3 2010 2010
dbSNP: rs3743078
rs3743078
CHRNA3
7 0.807 0.160 15 78602417 intron variant C/A;G snv 0.700 1.000 3 2010 2010
dbSNP: rs6495309
rs6495309
CHRNA3 ; CHRNB4
10 0.807 0.080 15 78622903 upstream gene variant C/A;T snv 0.700 1.000 3 2010 2010
dbSNP: rs684513
rs684513
CHRNA5
5 0.925 0.080 15 78566058 intron variant C/G;T snv 0.700 1.000 3 2010 2010
dbSNP: rs7177514
rs7177514
CHRNA3
6 0.882 0.080 15 78615064 intron variant C/G;T snv 0.700 1.000 3 2010 2010
dbSNP: rs8042059
rs8042059
CHRNA3
6 0.882 0.080 15 78615517 intron variant A/C;T snv 0.700 1.000 3 2010 2010
dbSNP: rs9788682
rs9788682
HYKK
2 15 78510244 intron variant G/A;T snv 0.700 1.000 3 2010 2010
dbSNP: rs11072768
rs11072768
CHRNB4
4 0.882 0.080 15 78637136 intron variant T/C;G snv 0.700 1.000 2 2010 2010
dbSNP: rs12903295
rs12903295
IREB2
3 15 78486630 intron variant A/C;G;T snv 0.700 1.000 2 2010 2010
dbSNP: rs12910627
rs12910627
CHRNB4 ; LOC105370913 ; LOC112268142
3 15 78702591 intron variant G/A;C snv 0.700 1.000 2 2010 2010
dbSNP: rs1329650
rs1329650
HECTD2-AS1
6 0.882 0.080 10 91588363 regulatory region variant G/A;T snv 0.700 1.000 2 2010 2012
dbSNP: rs1504550
rs1504550
IREB2
3 15 78473908 3 prime UTR variant A/G;T snv 0.700 1.000 2 2010 2010
dbSNP: rs17405217
rs17405217
IREB2
3 15 78438807 non coding transcript exon variant C/G;T snv 0.700 1.000 2 2010 2010
dbSNP: rs17483929
rs17483929
IREB2
3 15 78450034 intron variant G/A;T snv 0.700 1.000 2 2010 2010
dbSNP: rs17484235
rs17484235
IREB2
3 15 78469072 intron variant C/A;G;T snv 0.700 1.000 2 2010 2010
dbSNP: rs2938671
rs2938671
IREB2
2 15 78440412 intron variant A/G;T snv 0.700 1.000 2 2010 2010
dbSNP: rs3813565
rs3813565
CHRNB4 ; LOC105370913
6 0.851 0.080 15 78727268 splice region variant G/A;T snv 0.700 1.000 2 2010 2010
dbSNP: rs4887053
rs4887053 		4 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 0.700 1.000 2 2010 2010
dbSNP: rs569207
rs569207
CHRNA5
3 15 78580777 intron variant C/G;T snv 0.34 0.700 1.000 2 2010 2010