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: rs6495308
rs6495308
CHRNA3
8 0.851 0.160 15 78615314 intron variant T/C snv 0.29 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: rs7163730
rs7163730
HYKK
3 15 78522339 intron variant A/G snv 0.25 0.700 1.000 3 2010 2010
dbSNP: rs7164594
rs7164594
HYKK
2 15 78510715 intron variant C/T snv 0.32 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: rs8042374
rs8042374
CHRNA3
10 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.700 1.000 3 2010 2010
dbSNP: rs938682
rs938682
CHRNA3
7 0.851 0.080 15 78604205 intron variant G/A snv 0.72 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: rs1021071
rs1021071
CHRNB4 ; LOC112268142
3 15 78675837 intron variant G/C snv 0.28 0.700 1.000 2 2010 2010
dbSNP: rs10519203
rs10519203
HYKK
8 0.851 0.080 15 78521704 intron variant G/A snv 0.67 0.700 1.000 2 2010 2010
dbSNP: rs1062980
rs1062980
IREB2
8 0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 0.700 1.000 2 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: rs11072774
rs11072774
CHRNB4 ; LOC112268142
1 15 78660355 intron variant C/T snv 0.20 0.700 1.000 2 2010 2010
dbSNP: rs11072785
rs11072785
CHRNB4 ; LOC112268142
3 15 78675887 intron variant C/T snv 0.28 0.700 1.000 2 2010 2010
dbSNP: rs11072787
rs11072787
CHRNB4 ; LOC112268142
1 15 78680635 intron variant T/C snv 0.34 0.700 1.000 2 2010 2010
dbSNP: rs11072791
rs11072791
CHRNB4 ; LOC105370913 ; LOC112268142
3 15 78704734 intron variant C/A snv 0.29 0.700 1.000 2 2010 2010
dbSNP: rs11629637
rs11629637
CHRNB4 ; LOC105370913
3 15 78726682 intron variant C/T snv 0.31 0.700 1.000 2 2010 2010
dbSNP: rs11634042
rs11634042
MORF4L1 ; ADAMTS7
4 0.882 0.120 15 78813008 intron variant C/T snv 0.33 0.700 1.000 2 2010 2010
dbSNP: rs11634351
rs11634351
CHRNB4
3 15 78652376 intron variant G/A snv 0.28 0.700 1.000 2 2010 2010
dbSNP: rs11636605
rs11636605
CHRNB4
1 15 78636536 intron variant A/G snv 0.63 0.700 1.000 2 2010 2010
dbSNP: rs11638372
rs11638372
CHRNB4 ; LOC112268142
5 0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 0.700 1.000 2 2010 2010
dbSNP: rs11638490
rs11638490
CHRNB4 ; LOC105370913 ; LOC112268142
3 15 78715608 intron variant C/T snv 0.32 0.700 1.000 2 2010 2010
dbSNP: rs11638830
rs11638830
CHRNB4
3 15 78655977 intron variant G/C snv 0.28 0.700 1.000 2 2010 2010