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: rs17522122
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs2239647
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 4 2018 2019
dbSNP: rs12885221
rs12885221
AKAP6
14 32809804 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 3 2018 2019
dbSNP: rs2383377
rs2383377
AKAP6
1.000 0.040 14 32788708 intron variant G/A snv 0.13
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs10147849
rs10147849
AKAP6
14 32835225 3 prime UTR variant T/C snv 0.46
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs142370491
rs142370491
AKAP6
1.000 0.040 14 32749087 intron variant T/C snv 1.1E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2019 2019
dbSNP: rs17522122
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41
CUI: C4086152
Disease: Childhood Astrocytoma
Childhood Astrocytoma 		0.010 1.000 1 2019 2019
dbSNP: rs17522122
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		0.010 1.000 1 2019 2019
dbSNP: rs2143975
rs2143975
AKAP6
14 32828192 intron variant C/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2239647
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs2239647
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2239647
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2019 2019
dbSNP: rs2239647
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65
CUI: C0555198
Disease: Malignant Glioma
Malignant Glioma 		0.010 1.000 1 2019 2019
dbSNP: rs2239647
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65
CUI: C4722099
Disease: High grade glioma
High grade glioma 		0.010 1.000 1 2019 2019
dbSNP: rs4261436
rs4261436
AKAP6
0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43
CUI: C4086152
Disease: Childhood Astrocytoma
Childhood Astrocytoma 		0.010 1.000 1 2019 2019
dbSNP: rs4261436
rs4261436
AKAP6
0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		0.010 1.000 1 2019 2019
dbSNP: rs4261436
rs4261436
AKAP6
0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs1957021
rs1957021
AKAP6
1.000 0.080 14 32455299 intron variant T/A;C snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 2 2018 2018
dbSNP: rs7146202
rs7146202
AKAP6
14 32834311 3 prime UTR variant A/G snv 0.46
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2018 2018
dbSNP: rs10133551
rs10133551
AKAP6
14 32813026 intron variant T/C snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs1051695
rs1051695
AKAP6
14 32823916 missense variant A/G snv 0.59 0.64
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs11156751
rs11156751
AKAP6
1.000 0.080 14 32521231 intron variant T/C snv 0.27
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs1279143
rs1279143
AKAP6
14 32705894 intron variant A/G snv 0.41
CUI: C0201973
Disease: Creatine kinase measurement
Creatine kinase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1955513
rs1955513
AKAP6
0.925 0.120 14 32706736 intron variant T/G snv 0.11
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		0.010 1.000 1 2018 2018
dbSNP: rs1955513
rs1955513
AKAP6
0.925 0.120 14 32706736 intron variant T/G snv 0.11
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		0.010 1.000 1 2018 2018