FXR1, FMR1 autosomal homolog 1, 8087

N. diseases: 53; N. variants: 7
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: rs1805576
rs1805576 		1.000 0.040 3 180949777 intron variant C/G;T snv 0.24
CUI: C0013473
Disease: Eating Disorders
Eating Disorders 		Mental Disorders 0.710 1.000 1 2016 2016
dbSNP: rs34796896
rs34796896 		1.000 0.040 3 180905467 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 3 2018 2019
dbSNP: rs13076861
rs13076861 		1.000 0.040 3 180969810 intron variant T/A snv 0.17
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs13076861
rs13076861 		1.000 0.040 3 180969810 intron variant T/A snv 0.17
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs13096210
rs13096210 		1.000 0.040 3 180881530 intron variant C/T snv 6.3E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs1805576
rs1805576 		1.000 0.040 3 180949777 intron variant C/G;T snv 0.24
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs1805576
rs1805576 		1.000 0.040 3 180949777 intron variant C/G;T snv 0.24
CUI: C0029587
Disease: Other eating disorders
Other eating disorders 		Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs2037370
rs2037370 		1.000 0.040 3 180868697 intron variant G/C snv 0.48
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs519618
rs519618 		3 180946882 intron variant C/T snv 4.9E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs496250
rs496250 		0.851 0.080 3 180909515 intron variant G/A snv 0.24
CUI: C0154409
Disease: Recurrent major depressive episodes
Recurrent major depressive episodes 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs496250
rs496250 		0.851 0.080 3 180909515 intron variant G/A snv 0.24
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2017 2017
dbSNP: rs496250
rs496250 		0.851 0.080 3 180909515 intron variant G/A snv 0.24
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2017 2017
dbSNP: rs496250
rs496250 		0.851 0.080 3 180909515 intron variant G/A snv 0.24
CUI: C0338831
Disease: Manic
Manic 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs496250
rs496250 		0.851 0.080 3 180909515 intron variant G/A snv 0.24
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2017 2017