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: rs3784169
rs3784169
AKAP6
0.925 0.040 14 32333549 intron variant T/C snv 6.3E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs927062
rs927062
AKAP6
0.925 0.120 14 32625843 intron variant A/G snv 0.22
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		0.010 1.000 1 2018 2018
dbSNP: rs927062
rs927062
AKAP6
0.925 0.120 14 32625843 intron variant A/G snv 0.22
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		0.010 1.000 1 2018 2018
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