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: rs11771799
rs11771799
PILRB ; STAG3L5P-PVRIG2P-PILRB
7 100358813 missense variant T/A;C;G snv 4.3E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs151288400
rs151288400
PILRB ; STAG3L5P-PVRIG2P-PILRB
7 100360372 intron variant AG/- delins 0.16
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs35305377
rs35305377
PMS2P1 ; STAG3L5P ; STAG3L5P-PVRIG2P-PILRB
1.000 0.080 7 100341332 intron variant G/A snv 0.56
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
dbSNP: rs7384878
rs7384878
PMS2P1 ; STAG3L5P ; STAG3L5P-PVRIG2P-PILRB
7 100334426 intron variant C/T snv 0.72
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs7384878
rs7384878
PMS2P1 ; STAG3L5P ; STAG3L5P-PVRIG2P-PILRB
7 100334426 intron variant C/T snv 0.72
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019