CCNH, cyclin H, 902

N. diseases: 83; N. variants: 37
Disease: BASAL CELL CARCINOMA, SOMATIC ×
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: rs137853214
rs137853214 		0.925 0.040 5 87349304 missense variant G/T snv
CUI: C3838465
Disease: BASAL CELL CARCINOMA, SOMATIC
BASAL CELL CARCINOMA, SOMATIC 		0.700 0
dbSNP: rs137853215
rs137853215 		0.925 0.040 5 87349309 missense variant A/G snv
CUI: C3838465
Disease: BASAL CELL CARCINOMA, SOMATIC
BASAL CELL CARCINOMA, SOMATIC 		0.700 0
dbSNP: rs137853216
rs137853216 		0.925 0.040 5 87349312 missense variant A/G snv
CUI: C3838465
Disease: BASAL CELL CARCINOMA, SOMATIC
BASAL CELL CARCINOMA, SOMATIC 		0.700 0