rs1744297, ASPG

N. diseases: 12
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Alanine measurement
CUI: C0523459
Disease: Alanine measurement
3 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Asparagine measurement
CUI: C0523516
Disease: Asparagine measurement
4 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
blood phenylalanine measurement by Guthrie microbiologic assay
7 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Glutamine measurement
CUI: C0302274
Disease: Glutamine measurement
5 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Histidine measurement
CUI: C0523697
Disease: Histidine measurement
2 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Lysine measurement
CUI: C0523760
Disease: Lysine measurement
3 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Methionine measurement
CUI: C0428210
Disease: Methionine measurement
4 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Serine measurement
CUI: C0523888
Disease: Serine measurement
18 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Threonine measurement
CUI: C0523920
Disease: Threonine measurement
5 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Tryptophan measurement
CUI: C0523957
Disease: Tryptophan measurement
3 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
Tyrosine measurement
CUI: C0337446
Disease: Tyrosine measurement
11 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019