Gene: TCTA ×
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: rs6784820
rs6784820
RHOA ; TCTA
1 1.000 0.040 3 49413431 intron variant A/G snv 0.40 0.700 1.000 1 2008 2008
dbSNP: rs6997
rs6997
AMT ; TCTA
1 1.000 0.040 3 49416401 3 prime UTR variant C/T snv 0.30 0.700 1.000 1 2007 2007