rs2238732, PRODH

N. diseases: 7
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.
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 22 18927834 intron variant C/G;T snv 0.700 1.000 2 2015 2019
Alanine measurement
CUI: C0523459
Disease: Alanine measurement
3 22 18927834 intron variant C/G;T snv 0.700 1.000 1 2019 2019
blood phenylalanine measurement by Guthrie microbiologic assay
CUI: C0202174
Disease: blood phenylalanine measurement by Guthrie microbiologic assay
7 22 18927834 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Leucine measurement
CUI: C0428209
Disease: Leucine measurement
3 22 18927834 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Proline measurement
CUI: C0523852
Disease: Proline measurement
3 22 18927834 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Threonine measurement
CUI: C0523920
Disease: Threonine measurement
5 22 18927834 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Tyrosine measurement
CUI: C0337446
Disease: Tyrosine measurement
11 22 18927834 intron variant C/G;T snv 0.700 1.000 1 2019 2019