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: rs7255066
rs7255066
PVR ; LOC107985305
1.000 0.080 19 44642803 intron variant T/C snv 0.43
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs203709
rs203709
PVR ; LOC107985305
1.000 0.080 19 44658298 intron variant T/A snv 0.43
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 2 2018 2019
dbSNP: rs10426401
rs10426401
PVR ; LOC107985305
1.000 0.080 19 44644419 intron variant T/G snv 0.32
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs10426401
rs10426401
PVR ; LOC107985305
1.000 0.080 19 44644419 intron variant T/G snv 0.32
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11540084
rs11540084
PVR ; LOC107985305
19 44644040 5 prime UTR variant G/T snv 0.26
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs203710
rs203710
PVR ; LOC107985305
19 44658770 missense variant G/A snv 1.4E-02
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs28483039
rs28483039
PVR ; LOC107985305
19 44645964 intron variant G/A snv 0.32
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs56261258
rs56261258
PVR ; LOC107985305
1.000 0.080 19 44646342 intron variant T/C snv 0.92
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
dbSNP: rs7255066
rs7255066
PVR ; LOC107985305
1.000 0.080 19 44642803 intron variant T/C snv 0.43
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs73048339
rs73048339
PVR ; LOC107985305
19 44642563 intron variant T/C snv 3.3E-03
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016