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: rs5743708
rs5743708
TLR2
98 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 0.020 1.000 2 2005 2015
dbSNP: rs17850869
rs17850869
IST1 ; ZNF821 ; ATXN1L
1 1.000 0.040 16 71860078 synonymous variant C/T snv 9.7E-03 9.6E-03 0.010 1.000 1 2015 2015
dbSNP: rs41289586
rs41289586
ANO10
3 0.882 0.160 3 43577066 missense variant C/T snv 1.8E-02 1.9E-02 0.010 1.000 1 2015 2015
dbSNP: rs5743618
rs5743618
TLR1
25 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 0.010 1.000 1 2015 2015