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: rs2247870
rs2247870
ADGRV1
1.000 0.040 5 90855772 missense variant G/A snv 0.54 0.45
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs11744148
rs11744148
ADGRV1
5 90933990 intron variant G/A snv 0.18
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs13357230
rs13357230
ADGRV1 ; LUCAT1
5 91115255 intron variant A/G snv 5.8E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2247419
rs2247419
ADGRV1
1.000 0.040 5 90859597 intron variant A/G snv 0.57
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs3105793
rs3105793
ADGRV1
5 90930244 intron variant G/A snv 0.25
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4489092
rs4489092
ADGRV1 ; LUCAT1
5 91124827 intron variant G/T snv 0.49
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4916831
rs4916831
ADGRV1
1.000 0.040 5 90916459 intron variant A/G snv 0.44
CUI: C1706410
Disease: Atopic IgE-mediated allergic disorder
Atopic IgE-mediated allergic disorder 		0.700 1.000 1 2018 2018
dbSNP: rs57190680
rs57190680
ADGRV1
5 90910368 intron variant C/A snv 0.23
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs59661306
rs59661306
ADGRV1 ; LUCAT1
1.000 0.080 5 91087644 intron variant A/G snv 0.18
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs62374016
rs62374016
ADGRV1
5 90915456 intron variant T/C snv 0.25
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs6860111
rs6860111
ADGRV1
5 90967764 intron variant T/G snv 0.50
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs7449334
rs7449334
ADGRV1
1.000 0.040 5 91046595 intron variant G/A;C snv 0.76
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2019 2019
dbSNP: rs7449334
rs7449334
ADGRV1
1.000 0.040 5 91046595 intron variant G/A;C snv 0.76
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2019 2019
dbSNP: rs74501188
rs74501188
ADGRV1
1.000 0.080 5 90931162 5 prime UTR variant G/A snv 0.17
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung 		0.700 1.000 1 2017 2017