Gene: CHRNB4 ×
Source: GWASCAT ×
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: rs1021071
rs1021071
CHRNB4 ; LOC112268142
2 15 78675837 intron variant G/C snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs10851907
rs10851907
CHRNB4
4 1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 0.700 1.000 1 2015 2015
dbSNP: rs11072785
rs11072785
CHRNB4 ; LOC112268142
2 15 78675887 intron variant C/T snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs11072790
rs11072790
CHRNB4 ; LOC105370913 ; LOC112268142
2 15 78699683 intron variant C/T snv 0.31 0.700 1.000 1 2015 2015
dbSNP: rs11072791
rs11072791
CHRNB4 ; LOC105370913 ; LOC112268142
2 15 78704734 intron variant C/A snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs11072792
rs11072792
CHRNB4 ; LOC105370913 ; LOC112268142
2 15 78707569 intron variant A/G snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs113134286
rs113134286
CHRNB4 ; LOC105370913
2 15 78720546 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11629637
rs11629637
CHRNB4 ; LOC105370913
2 15 78726682 intron variant C/T snv 0.31 0.700 1.000 1 2015 2015
dbSNP: rs11633178
rs11633178
CHRNB4
2 15 78652196 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11634351
rs11634351
CHRNB4
2 15 78652376 intron variant G/A snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs11634543
rs11634543
CHRNB4 ; LOC105370913 ; LOC112268142
2 15 78713162 intron variant C/T snv 0.32 0.700 1.000 1 2015 2015
dbSNP: rs11638372
rs11638372
CHRNB4 ; LOC112268142
2 0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs11638490
rs11638490
CHRNB4 ; LOC105370913 ; LOC112268142
2 15 78715608 intron variant C/T snv 0.32 0.700 1.000 1 2015 2015
dbSNP: rs11638830
rs11638830
CHRNB4
2 15 78655977 intron variant G/C snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs11639372
rs11639372
CHRNB4 ; LOC112268142
4 0.925 0.080 15 78674313 intron variant C/T snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs12440014
rs12440014
CHRNB4
2 15 78634384 intron variant C/G snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs12441088
rs12441088
CHRNB4
2 15 78635922 intron variant G/T snv 0.69 0.700 1.000 1 2015 2015
dbSNP: rs12593950
rs12593950
CHRNB4
2 15 78628593 intron variant G/C snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs12899135
rs12899135
CHRNB4 ; LOC112268142
2 15 78662037 intron variant A/G snv 0.27 0.700 1.000 1 2015 2015
dbSNP: rs12901913
rs12901913
CHRNB4 ; LOC112268142
2 15 78689006 intron variant C/T snv 0.27 0.700 1.000 1 2015 2015
dbSNP: rs12902602
rs12902602
CHRNB4 ; LOC112268142
4 15 78675059 intron variant A/G snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs12910627
rs12910627
CHRNB4 ; LOC105370913 ; LOC112268142
2 15 78702591 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs17487223
rs17487223
CHRNB4
3 1.000 0.040 15 78631645 intron variant C/T snv 0.27 0.700 1.000 1 2015 2015
dbSNP: rs1996371
rs1996371
CHRNB4 ; LOC112268142
2 1.000 0.080 15 78664464 intron variant T/C snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs2170311
rs2170311
CHRNB4
2 15 78655269 intron variant G/A snv 0.29 0.700 1.000 1 2015 2015