Gene: PCAT1 ×
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: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
62 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.700 1.000 14 2007 2019
dbSNP: rs10505477
rs10505477
POU5F1B ; CASC8 ; PCAT1
31 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
dbSNP: rs7014346
rs7014346
POU5F1B ; CASC8 ; PCAT1
14 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
dbSNP: rs12682374
rs12682374
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
9 0.790 0.080 8 127398703 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7013278
rs7013278
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
10 0.776 0.080 8 127402647 intron variant T/C snv 0.59 0.700 1.000 1 2019 2019