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: rs141542003
rs141542003
TMEM126B
2 0.925 11 85636171 missense variant G/T snv 1.1E-03 1.0E-03 0.700 0
dbSNP: rs573006534
rs573006534
TMEM126B
1 1.000 11 85634279 missense variant G/A snv 8.4E-05; 8.8E-05 7.0E-05 0.700 0
dbSNP: rs886037835
rs886037835
TMEM126B
2 1.000 11 85635669 frameshift variant A/- delins 0.700 0
dbSNP: rs886037857
rs886037857
TMEM126B
1 1.000 11 85634090 stop gained C/T snv 0.700 0