NTAN1, N-terminal asparagine amidase, 123803

N. diseases: 8; N. variants: 13
Disease: Serum albumin measurement ×
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: rs1136001
rs1136001 		16 15038117 missense variant G/A;T snv 4.0E-06; 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12928099
rs12928099 		16 15056648 intron variant C/A snv 0.20
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs14347
rs14347 		16 15040032 synonymous variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16966953
rs16966953 		16 15041997 intron variant A/G snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2740
rs2740 		16 15038251 3 prime UTR variant A/C;G snv 0.33
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34614532
rs34614532 		16 15039051 intron variant T/C snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34955778
rs34955778 		16 15045737 non coding transcript exon variant T/C snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4985154
rs4985154 		16 15037785 3 prime UTR variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012