Source: CURATED

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: rs10520597
rs10520597
AKAP13
15 85627024 intron variant G/A snv 0.27
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12907384
rs12907384
AKAP13
15 85732769 intron variant T/A;C snv
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs12909648
rs12909648
AKAP13
15 85681339 intron variant G/A snv 0.40
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs12909648
rs12909648
AKAP13
15 85681339 intron variant G/A snv 0.40
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs16941432
rs16941432
AKAP13
15 85559945 intron variant A/G snv 0.37
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		0.700 1.000 1 2013 2013
dbSNP: rs2169876
rs2169876
AKAP13
15 85542545 intron variant T/A;C snv
CUI: C0877208
Disease: Peripartum cardiomyopathy
Peripartum cardiomyopathy 		0.700 1.000 1 2011 2011
dbSNP: rs2169877
rs2169877
AKAP13
15 85542571 intron variant G/A snv 0.70
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		0.700 1.000 1 2013 2013
dbSNP: rs2880765
rs2880765
AKAP13
1.000 0.040 15 85513231 intron variant A/T snv 0.48
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs338533
rs338533
AKAP13
15 85708862 intron variant G/T snv 0.24
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs56241813
rs56241813
AKAP13
15 85721280 intron variant G/A snv 7.0E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs62022112
rs62022112
AKAP13
15 85466377 intron variant T/G snv 0.14
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs62024517
rs62024517
AKAP13
15 85404905 intron variant T/C snv 0.14
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs74346567
rs74346567
AKAP13
15 85706491 intron variant G/A snv 6.1E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016