PTCH2, patched 2, 8643

N. diseases: 114; N. variants: 4
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: rs587776628
rs587776628 		1.000 1 44823064 splice region variant G/A snv
CUI: C3838465
Disease: BASAL CELL CARCINOMA, SOMATIC
BASAL CELL CARCINOMA, SOMATIC 		0.700 0