Source: ALL

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: rs11636101
rs11636101
CHRNA7
1.000 0.040 15 31981954 intron variant C/A snv 0.23
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11636810
rs11636810
CHRNA7
1.000 0.040 15 31988023 intron variant G/A snv 0.28
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11855355
rs11855355
CHRNA7
1.000 0.040 15 31992916 intron variant C/T snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11856897
rs11856897
CHRNA7
1.000 0.040 15 32000184 intron variant G/A snv 7.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs12438672
rs12438672
CHRNA7
1.000 0.040 15 32009123 intron variant G/A snv 7.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs12442690
rs12442690
CHRNA7
1.000 0.040 15 32009194 intron variant T/C snv 7.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs12595152
rs12595152
CHRNA7
1.000 0.040 15 32001084 intron variant C/T snv 0.55
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1304396
rs1304396
CHRNA7
1.000 0.040 15 31998287 intron variant C/T snv 0.55
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17228508
rs17228508
CHRNA7
1.000 0.040 15 31982116 intron variant C/T snv 7.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs7181544
rs7181544
CHRNA7
1.000 0.040 15 32002759 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs8038654
rs8038654
CHRNA7
1.000 0.040 15 31992661 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1566846736
rs1566846736
CHRNA7
15 32111789 splice acceptor variant G/A snv
CUI: C2751729
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7 		0.700 0
dbSNP: rs1339926621
rs1339926621
CHRNA7
1.000 0.080 15 32153944 missense variant G/A snv 8.6E-06
CUI: C0024809
Disease: Marijuana Abuse
Marijuana Abuse 		0.010 1.000 1 2007 2007
dbSNP: rs1909884
rs1909884
CHRNA7
0.925 0.120 15 32147097 intron variant G/A snv 0.41
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		0.010 1.000 1 2006 2006
dbSNP: rs1909884
rs1909884
CHRNA7
0.925 0.120 15 32147097 intron variant G/A snv 0.41
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM 		0.010 1.000 1 2006 2006
dbSNP: rs2337506
rs2337506
CHRNA7
0.925 0.080 15 32053864 intron variant A/G snv 0.60
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.010 1.000 1 2017 2017
dbSNP: rs2337506
rs2337506
CHRNA7
0.925 0.080 15 32053864 intron variant A/G snv 0.60
CUI: C0497327
Disease: Dementia
Dementia 		0.010 1.000 1 2017 2017
dbSNP: rs2337980
rs2337980
CHRNA7
0.925 0.120 15 32151995 intron variant C/T snv 0.45
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM 		0.010 1.000 1 2006 2006
dbSNP: rs2337980
rs2337980
CHRNA7
0.925 0.120 15 32151995 intron variant C/T snv 0.45
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		0.010 1.000 1 2006 2006
dbSNP: rs28531779
rs28531779
CHRNA7 ; LOC105370940
1.000 0.040 15 32030401 intron variant G/C snv 3.2E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 < 0.001 1 2015 2015
dbSNP: rs3087454
rs3087454
CHRNA7 ; LOC105370940
1.000 0.040 15 32028764 intron variant C/A;G;T snv 0.58
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2009 2009
dbSNP: rs6494223
rs6494223
CHRNA7
0.882 0.120 15 32104256 intron variant C/T snv 0.43
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2015 2015
dbSNP: rs6494223
rs6494223
CHRNA7
0.882 0.120 15 32104256 intron variant C/T snv 0.43
CUI: C0011253
Disease: Delusions
Delusions 		0.010 1.000 1 2008 2008
dbSNP: rs6494223
rs6494223
CHRNA7
0.882 0.120 15 32104256 intron variant C/T snv 0.43
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.010 1.000 1 2010 2010
dbSNP: rs7178176
rs7178176
CHRNA7
15 32151612 intron variant C/T snv 0.18
CUI: C0012833
Disease: Dizziness
Dizziness 		0.010 1.000 1 2014 2014