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: rs7225002
rs7225002
0.925 0.080 17 46111701 intron variant A/G snv 0.39
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs7225002
rs7225002
0.925 0.080 17 46111701 intron variant A/G snv 0.39
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs7225002
rs7225002
0.925 0.080 17 46111701 intron variant A/G snv 0.39
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs7225002
rs7225002
0.925 0.080 17 46111701 intron variant A/G snv 0.39
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs7225002
rs7225002
0.925 0.080 17 46111701 intron variant A/G snv 0.39
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs7225002
rs7225002
0.925 0.080 17 46111701 intron variant A/G snv 0.39
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2018 2018
dbSNP: rs7225002
rs7225002
0.925 0.080 17 46111701 intron variant A/G snv 0.39
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.700 1.000 1 2018 2018