Gene: MME ×
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: rs3736187
rs3736187
MME
1 1.000 0.080 3 155168489 splice region variant T/C snv 0.10 0.12 0.020 1.000 2 2004 2014
dbSNP: rs989692
rs989692
MME
1 1.000 0.080 3 155083576 5 prime UTR variant T/A;C snv 0.020 0.500 2 2004 2014
dbSNP: rs1327722411
rs1327722411
MME
1 1.000 0.080 3 155084188 synonymous variant G/A snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs1816558
rs1816558
MME
1 1.000 0.080 3 155125818 intron variant G/A snv 0.66 0.010 1.000 1 2016 2016
dbSNP: rs1836915
rs1836915
MME
1 1.000 0.080 3 155091313 intron variant T/C snv 0.12 0.010 1.000 1 2007 2007