Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6939340
rs6939340
0.851 0.160 6 22139775 intron variant A/G snv 0.62
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
0.840 1.000 1 2008 2017
dbSNP: rs4712653
rs4712653
0.882 0.080 6 22125735 intron variant T/C;G snv
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
0.830 1.000 2 2008 2017
dbSNP: rs9295536
rs9295536
0.882 0.080 6 22131700 intron variant C/A snv 0.58
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
0.830 1.000 2 2008 2017
dbSNP: rs1928168
rs1928168
6 22017509 intron variant T/C snv 0.36
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2012 2012
dbSNP: rs1928168
rs1928168
6 22017509 intron variant T/C snv 0.36
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding)
0.700 1.000 1 2011 2011
dbSNP: rs1928168
rs1928168
6 22017509 intron variant T/C snv 0.36
CUI: C0231921
Disease: Pulmonary function
Pulmonary function
0.700 1.000 1 2011 2011
dbSNP: rs2078543
rs2078543
6 21996631 intron variant A/G snv 0.69
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2012 2012
dbSNP: rs4712652
rs4712652
1.000 0.080 6 22078386 intron variant G/A snv 0.64
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
0.700 1.000 1 2010 2010
dbSNP: rs6939340
rs6939340
0.851 0.160 6 22139775 intron variant A/G snv 0.62
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010