Source: CURATED

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: rs1554774973
rs1554774973
NTRK2
1.000 0.120 9 84955504 missense variant C/T snv
CUI: C3151303
Disease: Obesity, Hyperphagia, and Developmental Delay
Obesity, Hyperphagia, and Developmental Delay 		0.800 1.000 3 2004 2017
dbSNP: rs121434633
rs121434633
NTRK2
0.925 0.120 9 84955510 missense variant A/G snv
CUI: C3151303
Disease: Obesity, Hyperphagia, and Developmental Delay
Obesity, Hyperphagia, and Developmental Delay 		0.800 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C4693367
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58 		0.800 0
dbSNP: rs1187352
rs1187352
NTRK2
0.925 0.040 9 84678542 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs1211166
rs1211166
NTRK2
9 84671077 intron variant G/A snv 0.77
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013
dbSNP: rs1211166
rs1211166
NTRK2
9 84671077 intron variant G/A snv 0.77
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2013 2013
dbSNP: rs1573219
rs1573219
NTRK2
1.000 0.080 9 84772707 intron variant A/G snv 0.67
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2019 2019
dbSNP: rs2291506
rs2291506
NTRK2
9 85024933 3 prime UTR variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1085308029
rs1085308029
NTRK2
1.000 0.120 9 84752019 stop gained G/T snv
CUI: C3151303
Disease: Obesity, Hyperphagia, and Developmental Delay
Obesity, Hyperphagia, and Developmental Delay 		0.700 0
dbSNP: rs1324578301
rs1324578301
NTRK2
1.000 0.080 9 85020233 missense variant C/T snv 4.0E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C4476723
Disease: Anti-multiple nuclear dots antibody positivity
Anti-multiple nuclear dots antibody positivity 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C0036572
Disease: Seizures
Seizures 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C0027092
Disease: Myopia
Myopia 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C0238651
Disease: Ankle clonus
Ankle clonus 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C0018552
Disease: Hamartoma
Hamartoma 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C4022761
Disease: Reduced brain N-acetyl aspartate level by MRS
Reduced brain N-acetyl aspartate level by MRS 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C4025573
Disease: Increased muscle fatiguability
Increased muscle fatiguability 		0.700 0
dbSNP: rs886041091
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv
CUI: C0018681
Disease: Headache
Headache 		0.700 0