MLEC, malectin, 9761

N. diseases: 7; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10431385
rs10431385
12 120691079 intron variant T/C snv 0.41
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10431386
rs10431386
1.000 0.040 12 120691123 intron variant C/T snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs2005455
rs2005455
12 120690896 intron variant A/G snv 0.41
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs2005455
rs2005455
12 120690896 intron variant A/G snv 0.41
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs3829290
rs3829290
12 120688635 intron variant T/C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs7306541
rs7306541
12 120692243 intron variant A/G snv 0.25
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7976497
rs7976497
1.000 0.080 12 120697664 3 prime UTR variant T/C snv 0.60
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10431386
rs10431386
1.000 0.040 12 120691123 intron variant C/T snv 0.34
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7964786
rs7964786
1.000 0.040 12 120694297 intron variant C/T snv 7.3E-05; 0.43 0.49
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7976497
rs7976497
1.000 0.080 12 120697664 3 prime UTR variant T/C snv 0.60
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016