CHP1, calcineurin like EF-hand protein 1, 11261

N. diseases: 141; N. variants: 4
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: rs28374715
rs28374715 		1.000 0.040 15 41271752 intron variant A/G snv 0.25
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.800 1.000 3 2012 2017
dbSNP: rs16971721
rs16971721 		0.925 0.040 15 41259663 intron variant T/C snv 2.1E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs16971721
rs16971721 		0.925 0.040 15 41259663 intron variant T/C snv 2.1E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs7162503
rs7162503 		15 41255494 intron variant A/G snv 0.53
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs6492998
rs6492998 		1.000 0.040 15 41254433 intron variant G/A snv 0.65
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2011 2011