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: rs104894410
rs104894410
GJB2
6 0.807 0.320 13 20189407 missense variant C/G;T snv 0.010 1.000 1 2006 2006
dbSNP: rs104894415
rs104894415
GJB6
11 0.742 0.240 13 20223450 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs200830749
rs200830749
MPG
2 0.925 0.240 16 79470 missense variant G/C snv 4.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs752478137
rs752478137
IL23R ; C1orf141
2 0.925 0.240 1 67168187 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs773946331
rs773946331
TLR2
2 0.925 0.240 4 153702941 missense variant G/A snv 3.6E-05 3.5E-05 0.010 1.000 1 2017 2017