FOXK2, forkhead box K2, 3607

N. diseases: 32; N. variants: 8
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9898189
rs9898189 		17 82522640 intron variant C/A;G snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 3 2016 2019
dbSNP: rs9898189
rs9898189 		17 82522640 intron variant C/A;G snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 3 2016 2019
dbSNP: rs11077998
rs11077998 		17 82526070 intron variant G/C snv 0.43
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11653286
rs11653286 		17 82574240 intron variant T/C snv 0.59
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3751909
rs3751909 		17 82571950 non coding transcript exon variant G/C snv 5.8E-02
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs56979318
rs56979318 		17 82564842 intron variant A/T snv 0.44
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs62079673
rs62079673 		1.000 0.080 17 82597601 intron variant T/C snv 0.52
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs73371707
rs73371707 		17 82558360 intron variant G/A snv 6.2E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs786205510
rs786205510 		1.000 17 82619074 stop gained G/A snv
CUI: C4693816
Disease: NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES
NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES 		0.700 0