SNP Detail Info-rs7324177

Molecule type	Change	Amino acid[Codon]	SO Term
FGF14 transcript variant 3	NM_001321931.1:c.	N/A	Intron Variant
FGF14 transcript variant 4	NM_001321932.1:c.	N/A	Intron Variant
FGF14 transcript variant 5	NM_001321933.1:c.	N/A	Intron Variant
FGF14 transcript variant 6	NM_001321934.1:c.	N/A	Intron Variant
FGF14 transcript variant 7	NM_001321935.1:c.	N/A	Intron Variant
FGF14 transcript variant 8	NM_001321936.1:c.	N/A	Intron Variant
FGF14 transcript variant 9	NM_001321937.1:c.	N/A	Intron Variant
FGF14 transcript variant 10	NM_001321938.1:c.	N/A	Intron Variant
FGF14 transcript variant 11	NM_001321939.1:c.	N/A	Intron Variant
FGF14 transcript variant 12	NM_001321940.1:c.	N/A	Intron Variant
FGF14 transcript variant 13	NM_001321941.1:c.	N/A	Intron Variant
FGF14 transcript variant 14	NM_001321942.1:c.	N/A	Intron Variant
FGF14 transcript variant 15	NM_001321943.1:c.	N/A	Intron Variant
FGF14 transcript variant 16	NM_001321944.1:c.	N/A	Intron Variant
FGF14 transcript variant 17	NM_001321945.1:c.	N/A	Intron Variant
FGF14 transcript variant 18	NM_001321946.1:c.	N/A	Intron Variant
FGF14 transcript variant 19	NM_001321947.1:c.	N/A	Intron Variant
FGF14 transcript variant 20	NM_001321948.1:c.	N/A	Intron Variant
FGF14 transcript variant 21	NM_001321949.1:c.	N/A	Intron Variant
FGF14 transcript variant 2	NM_175929.2:c.	N/A	Intron Variant
FGF14 transcript variant 1	NM_004115.3:c.	N/A	Genic Upstream Transcript Variant

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	G=0.925	A=0.075
1000Genomes	American	Sub	694	G=1.000	A=0.000
1000Genomes	East Asian	Sub	1008	G=1.000	A=0.000
1000Genomes	Europe	Sub	1006	G=1.000	A=0.000
1000Genomes	Global	Study-wide	5008	G=0.980	A=0.020
1000Genomes	South Asian	Sub	978	G=1.000	A=0.000
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=1.000	A=0.000
The Genome Aggregation Database	African	Sub	8688	G=0.941	A=0.059
The Genome Aggregation Database	American	Sub	838	G=1.000	A=0.000
The Genome Aggregation Database	East Asian	Sub	1616	G=1.000	A=0.000
The Genome Aggregation Database	Europe	Sub	18456	G=0.999	A=0.000
The Genome Aggregation Database	Global	Study-wide	29900	G=0.982	A=0.017
The Genome Aggregation Database	Other	Sub	302	G=0.990	A=0.010
Trans-Omics for Precision Medicine	Global	Study-wide	29118	G=0.973	A=0.027
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.999	A=0.001

PMID	Title	Author	Journal
20201924	Genome-wide association study of alcohol dependence implicates a region on chromosome 11.	Edenberg HJ	Alcohol Clin Exp Res

SNP ID	p-value	Traits	Study
rs7324177	0.00035	alcohol dependence	20201924

Position (v37)	eGene	GeneID	Variant	p-value	TSS	Tissue
There is no eQTL annotation for this SNP

Probe ID	Position	Gene	beta	p-value
There is no meQTL annotation for this SNP

Chromosome	Start	End	Region	Distance ( -/+ : Up/Downstream )
chr13	102649508	102649644	E067	21909
chr13	102630341	102630429	E070	2742
chr13	102630648	102630761	E070	3049
chr13	102630964	102631033	E070	3365
chr13	102631080	102631393	E070	3481
chr13	102631448	102631595	E070	3849
chr13	102632225	102632319	E070	4626
chr13	102635351	102635472	E070	7752
chr13	102635931	102635981	E070	8332
chr13	102656327	102656416	E070	28728
chr13	102656661	102656808	E070	29062
chr13	102656914	102656964	E070	29315
chr13	102657787	102657852	E070	30188
chr13	102657877	102657951	E070	30278
chr13	102662767	102662831	E070	35168
chr13	102649329	102649445	E071	21730
chr13	102649508	102649644	E071	21909
chr13	102635351	102635472	E072	7752
chr13	102649329	102649445	E072	21730
chr13	102649508	102649644	E072	21909
chr13	102649329	102649445	E073	21730
chr13	102649508	102649644	E073	21909
chr13	102649329	102649445	E074	21730
chr13	102649508	102649644	E074	21909
chr13	102583261	102583311	E081	-44288
chr13	102583534	102583833	E081	-43766
chr13	102656661	102656808	E081	29062
chr13	102656914	102656964	E081	29315
chr13	102657787	102657852	E081	30188
chr13	102657877	102657951	E081	30278

rs7324177