Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0523459
Disease: Alanine measurement
Alanine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0337446
Disease: Tyrosine measurement
Tyrosine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0428210
Disease: Methionine measurement
Methionine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0523516
Disease: Asparagine measurement
Asparagine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0523957
Disease: Tryptophan measurement
Tryptophan measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0523920
Disease: Threonine measurement
Threonine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0302274
Disease: Glutamine measurement
Glutamine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0523697
Disease: Histidine measurement
Histidine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0202174
Disease: blood phenylalanine measurement by Guthrie microbiologic assay
blood phenylalanine measurement by Guthrie microbiologic assay 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0523760
Disease: Lysine measurement
Lysine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86
CUI: C0523888
Disease: Serine measurement
Serine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2282377
rs2282377
ASPG
1.000 0.080 14 104105483 intron variant C/G snv 0.12 0.12
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.700 1.000 1 2018 2018
dbSNP: rs2282377
rs2282377
ASPG
1.000 0.080 14 104105483 intron variant C/G snv 0.12 0.12
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.700 1.000 1 2018 2018
dbSNP: rs61997624
rs61997624
ASPG ; MIR203A
14 104116049 upstream gene variant C/T snv 0.12
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0.700 1.000 1 2019 2019
dbSNP: rs61997624
rs61997624
ASPG ; MIR203A
14 104116049 upstream gene variant C/T snv 0.12
CUI: C0523516
Disease: Asparagine measurement
Asparagine measurement 		0.700 1.000 1 2019 2019