CRY1, cryptochrome circadian regulator 1, 1407

N. diseases: 91; 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: rs184039278
rs184039278 		12 106992962 splice region variant T/C;G snv 4.6E-03
CUI: C3279991
Disease: DELAYED SLEEP PHASE DISORDER, SUSCEPTIBILITY TO
DELAYED SLEEP PHASE DISORDER, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs11113179
rs11113179 		0.925 0.080 12 107059007 intron variant C/T snv 8.8E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11113179
rs11113179 		0.925 0.080 12 107059007 intron variant C/T snv 8.8E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3809236
rs3809236 		1.000 0.080 12 107093269 5 prime UTR variant G/A;C snv 0.14
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs566794487
rs566794487 		12 106997986 missense variant A/C snv 3.6E-05
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2017 2017