Source: GWASCAT

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: rs896854
rs896854
TP53INP1 ; NDUFAF6
1.000 0.080 8 94948283 intron variant T/C snv 0.45
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.810 1.000 1 2010 2018
dbSNP: rs7845219
rs7845219
NDUFAF6
1.000 0.080 8 94925274 intron variant T/C snv 0.45
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 2 2014 2018
dbSNP: rs7818382
rs7818382
NDUFAF6
1.000 0.080 8 95041772 intron variant C/T snv 0.42
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2013 2013
dbSNP: rs7835379
rs7835379
NDUFAF6
8 94962852 intron variant G/A;C snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 2 2018 2019
dbSNP: rs10098778
rs10098778
NDUFAF6
1.000 0.080 8 94979792 intron variant C/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs10429294
rs10429294
NDUFAF6
8 94957094 intron variant C/T snv 0.50
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness 		0.700 1.000 1 2018 2018
dbSNP: rs12548367
rs12548367
NDUFAF6
8 94916974 intron variant C/A;T snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs12548874
rs12548874
NDUFAF6
8 94922936 intron variant C/A snv 0.40
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1320164
rs1320164
TP53INP1 ; NDUFAF6
1.000 0.080 8 94948539 intron variant G/A snv 0.45
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2019 2019
dbSNP: rs2011567
rs2011567
NDUFAF6
8 94959692 intron variant G/A;C snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs2599711
rs2599711
NDUFAF6
8 95059968 intron variant T/A snv 0.75
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs481887
rs481887
NDUFAF6
8 94955610 intron variant A/G snv 0.33
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs7818688
rs7818688
NDUFAF6
1.000 0.120 8 95011854 intron variant C/A;G snv
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs7818688
rs7818688
NDUFAF6
1.000 0.120 8 95011854 intron variant C/A;G snv
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.700 1.000 1 2015 2015
dbSNP: rs7818688
rs7818688
NDUFAF6
1.000 0.120 8 95011854 intron variant C/A;G snv
CUI: C0442874
Disease: Neuropathy
Neuropathy 		0.700 1.000 1 2015 2015
dbSNP: rs896847
rs896847
NDUFAF6
8 94960323 intron variant G/A snv 0.50
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs896854
rs896854
TP53INP1 ; NDUFAF6
1.000 0.080 8 94948283 intron variant T/C snv 0.45
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9297949
rs9297949
NDUFAF6
8 94957217 intron variant A/C snv 0.50
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018