Gene: CLPTM1L ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs401681
rs401681
CLPTM1L
42 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.800 1.000 16 2008 2018
dbSNP: rs380286
rs380286
CLPTM1L
8 0.776 0.200 5 1320132 intron variant G/A snv 0.47 0.710 1.000 3 2014 2019
dbSNP: rs421629
rs421629
CLPTM1L
2 0.925 0.160 5 1320021 intron variant G/A snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs402710
rs402710
CLPTM1L
18 0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38 0.100 1.000 13 2009 2018
dbSNP: rs31489
rs31489
CLPTM1L
10 0.763 0.320 5 1342599 intron variant C/A snv 0.41 0.050 1.000 5 2010 2014
dbSNP: rs451360
rs451360
CLPTM1L
5 0.827 0.200 5 1319565 intron variant C/A;T snv 0.020 1.000 2 2014 2014
dbSNP: rs465498
rs465498
CLPTM1L
9 0.776 0.200 5 1325688 non coding transcript exon variant A/G snv 0.46 0.020 1.000 2 2011 2015
dbSNP: rs31484
rs31484
CLPTM1L
4 0.851 0.160 5 1337791 intron variant A/T snv 0.51 0.010 1.000 1 2014 2014
dbSNP: rs31490
rs31490
CLPTM1L
8 0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06 0.010 1.000 1 2013 2013