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: rs16839481
rs16839481
UBA5 ; ACAD11 ; NPHP3-ACAD11
3 132660153 5 prime UTR variant G/A snv 1.1E-02
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0.700 1.000 1 2017 2017
dbSNP: rs16839481
rs16839481
UBA5 ; ACAD11 ; NPHP3-ACAD11
3 132660153 5 prime UTR variant G/A snv 1.1E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0.700 1.000 1 2017 2017
dbSNP: rs17348614
rs17348614
NPHP3 ; NPHP3-ACAD11
3 132692324 intron variant C/T snv 4.4E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs17348614
rs17348614
NPHP3 ; NPHP3-ACAD11
3 132692324 intron variant C/T snv 4.4E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs1869862
rs1869862
ACAD11 ; NPHP3-ACAD11
3 132582905 intron variant A/C snv 0.56
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs34116314
rs34116314
UBA5 ; ACAD11 ; NPHP3-ACAD11
3 132656496 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs41272321
rs41272321
ACAD11 ; NPHP3-ACAD11
3 132619502 missense variant T/C;G snv 8.6E-06; 0.11
CUI: C4553013
Disease: Chemokine (C-C Motif) Ligand 21 Measurement
Chemokine (C-C Motif) Ligand 21 Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs41272321
rs41272321
ACAD11 ; NPHP3-ACAD11
3 132619502 missense variant T/C;G snv 8.6E-06; 0.11
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs572076167
rs572076167
NPHP3 ; NPHP3-ACAD11
3 132716018 intron variant T/C;G snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018