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: rs1033962
rs1033962
PRTFDC1
1.000 0.040 10 24927877 intron variant C/T snv 0.33
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		0.700 1.000 1 2015 2015
dbSNP: rs10828723
rs10828723
PRTFDC1
10 24916129 intron variant T/C snv 0.26
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10828725
rs10828725
PRTFDC1
10 24929314 intron variant G/T snv 0.26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10828725
rs10828725
PRTFDC1
10 24929314 intron variant G/T snv 0.26
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11014271
rs11014271
PRTFDC1
10 24871573 intron variant C/T snv 0.12
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs11014285
rs11014285
PRTFDC1
10 24889935 intron variant G/A snv 0.11
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11014285
rs11014285
PRTFDC1
10 24889935 intron variant G/A snv 0.11
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs11014291
rs11014291
PRTFDC1
10 24909758 intron variant T/C snv 0.26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs11014296
rs11014296
PRTFDC1
10 24913109 intron variant C/T snv 0.26
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11818463
rs11818463
PRTFDC1
10 24934438 intron variant G/A;C snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs11818463
rs11818463
PRTFDC1
10 24934438 intron variant G/A;C snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs12266014
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs12266014
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs12266014
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12266014
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs12266014
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12266014
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs12266014
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs140884840
rs140884840
PRTFDC1
10 24911877 intron variant CAAACAAA/-;CAAA delins
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs151165649
rs151165649
PRTFDC1
10 24918312 intron variant G/A snv 6.9E-03
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.700 1.000 1 2017 2017
dbSNP: rs7394259
rs7394259
PRTFDC1
10 24877899 intron variant G/A snv 0.12
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs7905553
rs7905553
PRTFDC1
10 24911662 intron variant C/G;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs7905553
rs7905553
PRTFDC1
10 24911662 intron variant C/G;T snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019