GAL, galanin and GMAP prepropeptide, 51083

N. diseases: 226; N. variants: 3
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: rs1057517661
rs1057517661 		0.925 0.040 11 68685628 missense variant C/A;T snv
CUI: C4225318
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
EPILEPSY, FAMILIAL TEMPORAL LOBE, 8 		0.700 0
dbSNP: rs948854
rs948854 		0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.020 1.000 2 2010 2018
dbSNP: rs1057517661
rs1057517661 		0.925 0.040 11 68685628 missense variant C/A;T snv
CUI: C0014556
Disease: Epilepsy, Temporal Lobe
Epilepsy, Temporal Lobe 		Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs694066
rs694066 		1.000 0.040 11 68685517 intron variant G/A snv 0.15
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs948854
rs948854 		0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2018 2018
dbSNP: rs948854
rs948854 		0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs948854
rs948854 		0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2017 2017