Gene: MMP9 ×
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: rs17576
rs17576
MMP9
73 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.030 0.333 3 2005 2019
dbSNP: rs17577
rs17577
MMP9 ; SLC12A5-AS1
31 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 0.020 1.000 2 2013 2019
dbSNP: rs13925
rs13925
MMP9 ; SLC12A5-AS1
1 1.000 0.080 20 46016326 synonymous variant G/A snv 0.15 0.15 0.010 1.000 1 2018 2018
dbSNP: rs20544
rs20544
MMP9 ; SLC12A5-AS1
2 0.925 0.120 20 46016371 3 prime UTR variant C/T snv 0.43 0.44 0.010 1.000 1 2018 2018
dbSNP: rs3918242
rs3918242
MMP9
54 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 < 0.001 1 2019 2019
dbSNP: rs3918249
rs3918249
MMP9
6 0.807 0.200 20 46009497 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013