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: 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