Gene: TRGV11 ×
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: rs1860520
rs1860520
TRGV11
1 1.000 0.040 7 38291670 missense variant C/A snv 6.2E-02 0.19 0.700 1.000 1 2009 2009
dbSNP: rs1860521
rs1860521
TRGV11
1 1.000 0.040 7 38291903 missense variant C/T snv 6.5E-02 0.19 0.700 1.000 1 2009 2009