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: rs387907133
rs387907133
TMEM138
1 1.000 11 61368600 missense variant C/T snv 4.0E-06 0.800 1.000 2 2012 2015
dbSNP: rs387907132
rs387907132
TMEM138
1 1.000 11 61366203 missense variant A/G snv 2.4E-05 7.0E-06 0.800 1.000 1 2012 2012
dbSNP: rs387907134
rs387907134
TMEM138
1 1.000 11 61367998 missense variant G/A snv 0.800 1.000 1 2012 2012
dbSNP: rs387907135
rs387907135
TMEM138
1 1.000 11 61368609 missense variant A/G snv 4.0E-06 0.700 1.000 1 2012 2012