Gene: TCF19 ×
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: rs2073723
rs2073723
TCF19
2 0.925 0.160 6 31162301 intron variant T/C snv 0.78 0.700 1.000 1 2011 2011
dbSNP: rs3094187
rs3094187
TCF19 ; CCHCR1
5 0.925 0.120 6 31159167 5 prime UTR variant C/T snv 0.55 0.700 1.000 1 2011 2011