FGF20, fibroblast growth factor 20, 26281

N. diseases: 45; N. variants: 6
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: rs587777282
rs587777282 		1.000 8 16995708 frameshift variant C/- del
CUI: C3810359
Disease: RENAL HYPODYSPLASIA/APLASIA 2
RENAL HYPODYSPLASIA/APLASIA 2 		0.700 0
dbSNP: rs12720208
rs12720208 		0.925 0.040 8 16992890 3 prime UTR variant G/A snv 5.5E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.060 0.333 6 2009 2017
dbSNP: rs1721100
rs1721100 		0.925 0.040 8 16992989 3 prime UTR variant C/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.050 0.800 5 2004 2018
dbSNP: rs12720208
rs12720208 		0.925 0.040 8 16992890 3 prime UTR variant G/A snv 5.5E-02
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.010 1.000 1 2018 2018
dbSNP: rs12720208
rs12720208 		0.925 0.040 8 16992890 3 prime UTR variant G/A snv 5.5E-02
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs149242678
rs149242678 		1.000 0.040 8 17002089 5 prime UTR variant G/A;C snv
CUI: C0399526
Disease: Class III malocclusion
Class III malocclusion 		Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1721100
rs1721100 		0.925 0.040 8 16992989 3 prime UTR variant C/G;T snv
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs17550360
rs17550360 		1.000 0.040 8 16993092 missense variant C/A;T snv 4.0E-05; 5.8E-03
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1989754
rs1989754 		1.000 0.040 8 17000966 intron variant G/C snv 0.36
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2004 2004