CLPTM1L, CLPTM1 like, 81037

N. diseases: 110; N. variants: 20
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: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
Neoplasms 0.700 1.000 3 2009 2015
dbSNP: rs421284
rs421284
0.882 0.040 5 1325475 non coding transcript exon variant T/C;G snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
Neoplasms 0.700 1.000 2 2016 2019