NUTF2, nuclear transport factor 2, 10204

N. diseases: 11; N. variants: 5
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: rs2271293
rs2271293
1.000 0.040 16 67868167 intron variant G/A snv 0.11
High density lipoprotein measurement
0.800 1.000 3 2009 2019
dbSNP: rs2271293
rs2271293
1.000 0.040 16 67868167 intron variant G/A snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2009 2009
dbSNP: rs1124324
rs1124324
16 67863584 intron variant C/T snv 0.15
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs1124324
rs1124324
16 67863584 intron variant C/T snv 0.15
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11553287
rs11553287
16 67871504 3 prime UTR variant A/G snv 0.31
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2271293
rs2271293
1.000 0.040 16 67868167 intron variant G/A snv 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2271294
rs2271294
16 67868423 non coding transcript exon variant A/G;T snv 0.21
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs7198357
rs7198357
16 67850716 intron variant C/T snv 0.30
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012