CLPTM1L, CLPTM1 like, 81037

N. diseases: 110; N. variants: 20
Disease: Carcinoma, Basal Cell ×
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: rs401681
rs401681 		0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		Neoplasms 0.740 1.000 6 2009 2017
dbSNP: rs893729101
rs893729101 		1.000 0.040 5 1341708 missense variant T/C snv 2.1E-05
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		Neoplasms 0.010 1.000 1 2009 2009