Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12788102
rs12788102
MMP26 ; OR51F1
1.000 0.040 11 4769345 synonymous variant A/G snv 9.5E-02 9.6E-02
CUI: C0024530
Disease: Malaria
Malaria 		0.800 1.000 1 2013 2013
dbSNP: rs840716
rs840716
MMP26
11 4932232 intron variant G/T snv 8.3E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 2 2008 2011
dbSNP: rs10836955
rs10836955
MMP26 ; OR51G1
11 4924401 intron variant G/A snv 0.15
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs11035019
rs11035019
MMP26
11 4988333 intron variant C/T snv 2.6E-03 1.0E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11035019
rs11035019
MMP26
11 4988333 intron variant C/T snv 2.6E-03 1.0E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12271916
rs12271916
MMP26
11 4705648 intron variant G/A snv 0.16
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs12277512
rs12277512
MMP26
11 4827808 intron variant A/T snv 0.37
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs12279647
rs12279647
MMP26 ; OR51A8P
11 4832104 non coding transcript exon variant C/T snv 0.37
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs12788102
rs12788102
MMP26 ; OR51F1
1.000 0.040 11 4769345 synonymous variant A/G snv 9.5E-02 9.6E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs12789492
rs12789492
MMP26
1.000 0.040 11 4772889 intron variant C/T snv 9.6E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs12789492
rs12789492
MMP26
1.000 0.040 11 4772889 intron variant C/T snv 9.6E-02
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2013 2013
dbSNP: rs12801757
rs12801757
MMP26
1.000 0.040 11 4785824 intron variant A/G;T snv
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2013 2013
dbSNP: rs12802922
rs12802922
MMP26 ; OR51G2
11 4914380 3 prime UTR variant C/T snv 9.7E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs12806476
rs12806476
MMP26
1.000 0.040 11 4785642 intron variant T/G snv 9.6E-02
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2013 2013
dbSNP: rs12808215
rs12808215
MMP26
1.000 0.040 11 4786742 intron variant A/G snv 9.6E-02
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2013 2013
dbSNP: rs1594812
rs1594812
MMP26
1.000 0.040 11 4777979 intron variant T/G snv 9.6E-02
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2013 2013
dbSNP: rs16907254
rs16907254
MMP26
11 4909853 intron variant C/T snv 9.4E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs17227393
rs17227393
MMP26
11 4772319 intron variant T/C snv 0.11
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs17227484
rs17227484
MMP26
11 4772652 intron variant A/G snv 9.6E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs17227547
rs17227547
MMP26
11 4772963 intron variant A/G snv 9.6E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs17227978
rs17227978
MMP26 ; OR51N1P
1.000 0.040 11 4787195 non coding transcript exon variant G/A snv 9.6E-02
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2013 2013
dbSNP: rs17227978
rs17227978
MMP26 ; OR51N1P
1.000 0.040 11 4787195 non coding transcript exon variant G/A snv 9.6E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs17228092
rs17228092
MMP26
1.000 0.040 11 4789134 intron variant T/C snv 9.6E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs17228092
rs17228092
MMP26
1.000 0.040 11 4789134 intron variant T/C snv 9.6E-02
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2013 2013
dbSNP: rs17228176
rs17228176
MMP26
1.000 0.040 11 4790570 intron variant A/G snv 9.6E-02
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008