Gene: TNXB ×
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: rs776989258
rs776989258
CYP21A2 ; TNXB
6 0.807 0.280 6 32041093 missense variant C/G;T snv 5.5E-04 0.040 1.000 4 2000 2004
dbSNP: rs6445
rs6445
CYP21A2 ; TNXB
5 0.827 0.240 6 32041006 missense variant C/T snv 4.6E-03 5.2E-03 0.030 1.000 3 2000 2003
dbSNP: rs1245238711
rs1245238711
CYP21A2 ; TNXB
2 0.925 0.240 6 32040940 missense variant G/A snv 2.1E-05 0.010 1.000 1 2015 2015
dbSNP: rs1312209092
rs1312209092
CYP21A2 ; TNXB
2 0.925 0.240 6 32041068 missense variant G/A snv 0.010 1.000 1 2015 2015
dbSNP: rs151344504
rs151344504
CYP21A2 ; TNXB
2 0.925 0.240 6 32040926 missense variant G/A snv 7.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs202242769
rs202242769
CYP21A2 ; TNXB
2 0.925 0.240 6 32040723 missense variant G/A;C snv 0.010 1.000 1 2009 2009
dbSNP: rs56345590
rs56345590
TNXB
2 0.925 0.200 6 32042485 missense variant G/A;C snv 4.0E-06; 2.0E-05 0.010 < 0.001 1 2016 2016
dbSNP: rs759736443
rs759736443
CYP21A2 ; TNXB
3 0.882 0.240 6 32041096 missense variant C/T snv 2.1E-04; 2.7E-05 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs766099537
rs766099537
CYP21A2 ; TNXB
1 1.000 0.040 6 32041118 missense variant C/T snv 2.1E-05 3.5E-05 0.010 1.000 1 2019 2019