Gene: PTCSC2 ×
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: rs965513
rs965513
PTCSC2
15 0.742 0.200 9 97793827 intron variant A/G;T snv 0.100 0.917 12 2011 2017
dbSNP: rs1867277
rs1867277
FOXE1 ; PTCSC2
10 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.080 0.750 8 2011 2017
dbSNP: rs3758249
rs3758249
FOXE1 ; PTCSC2
3 0.882 0.200 9 97851858 intron variant T/C snv 0.63 0.010 1.000 1 2014 2014
dbSNP: rs894673
rs894673
PTCSC2
1 1.000 0.080 9 97849988 intron variant A/T snv 0.63 0.010 1.000 1 2015 2015
dbSNP: rs925489
rs925489
PTCSC2
6 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.010 1.000 1 2014 2014