Gene: MMP26 ×
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: rs12788102
rs12788102
MMP26 ; OR51F1
2 1.000 0.040 11 4769345 synonymous variant A/G snv 9.5E-02 9.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs12789492
rs12789492
MMP26
2 1.000 0.040 11 4772889 intron variant C/T snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs12801757
rs12801757
MMP26
1 1.000 0.040 11 4785824 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs12806476
rs12806476
MMP26
1 1.000 0.040 11 4785642 intron variant T/G snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs12808215
rs12808215
MMP26
1 1.000 0.040 11 4786742 intron variant A/G snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs1594812
rs1594812
MMP26
1 1.000 0.040 11 4777979 intron variant T/G snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs17227978
rs17227978
MMP26 ; OR51N1P
2 1.000 0.040 11 4787195 non coding transcript exon variant G/A snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs17228092
rs17228092
MMP26
2 1.000 0.040 11 4789134 intron variant T/C snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs17228176
rs17228176
MMP26
2 1.000 0.040 11 4790570 intron variant A/G snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs17228183
rs17228183
MMP26
2 1.000 0.040 11 4790653 intron variant G/A snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs17325567
rs17325567
MMP26 ; OR51N1P
2 1.000 0.040 11 4786903 non coding transcript exon variant T/C snv 9.6E-02 0.700 1.000 1 2013 2013