SNP Detail Info-rs7208821

Molecule type	Change	Amino acid[Codon]	SO Term
MYH10 transcript variant 1	NM_001256012.1:c.	N/A	Intron Variant
MYH10 transcript variant 3	NM_001256095.1:c.	N/A	Intron Variant
MYH10 transcript variant 2	NM_005964.3:c.	N/A	Intron Variant
MYH10 transcript variant X10	XM_011523875.2:c.	N/A	Intron Variant
MYH10 transcript variant X1	XM_011523878.2:c.	N/A	Intron Variant
MYH10 transcript variant X2	XM_011523879.2:c.	N/A	Intron Variant
MYH10 transcript variant X3	XM_011523880.2:c.	N/A	Intron Variant
MYH10 transcript variant X4	XM_017024677.1:c.	N/A	Intron Variant
MYH10 transcript variant X5	XM_017024678.1:c.	N/A	Intron Variant
MYH10 transcript variant X6	XM_017024679.1:c.	N/A	Intron Variant
MYH10 transcript variant X7	XM_017024680.1:c.	N/A	Intron Variant
MYH10 transcript variant X8	XM_017024681.1:c.	N/A	Intron Variant
MYH10 transcript variant X9	XM_017024682.1:c.	N/A	Intron Variant

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	C=0.970	T=0.030
1000Genomes	American	Sub	694	C=0.980	T=0.020
1000Genomes	East Asian	Sub	1008	C=0.807	T=0.193
1000Genomes	Europe	Sub	1006	C=0.978	T=0.022
1000Genomes	Global	Study-wide	5008	C=0.944	T=0.056
1000Genomes	South Asian	Sub	978	C=0.990	T=0.010
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.976	T=0.024
The Genome Aggregation Database	African	Sub	8722	C=0.967	T=0.033
The Genome Aggregation Database	American	Sub	838	C=0.990	T=0.010
The Genome Aggregation Database	East Asian	Sub	1620	C=0.810	T=0.190
The Genome Aggregation Database	Europe	Sub	18492	C=0.965	T=0.034
The Genome Aggregation Database	Global	Study-wide	29974	C=0.958	T=0.041
The Genome Aggregation Database	Other	Sub	302	C=0.970	T=0.030
Trans-Omics for Precision Medicine	Global	Study-wide	29118	C=0.972	T=0.027
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.977	T=0.023

PMID	Title	Author	Journal
21314694	Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.	Kendler KS	Alcohol Clin Exp Res

SNP ID	p-value	Traits	Study
rs7208821	0.000741	alcohol dependence	21314694

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 )
chr17	8509571	8510185	E067	32828
chr17	8510192	8510258	E067	33449
chr17	8524959	8525238	E067	48216
chr17	8525281	8525535	E067	48538
chr17	8525650	8525762	E067	48907
chr17	8509571	8510185	E068	32828
chr17	8510192	8510258	E068	33449
chr17	8509571	8510185	E069	32828
chr17	8510192	8510258	E069	33449
chr17	8466462	8466611	E070	-10132
chr17	8484195	8485211	E070	7452
chr17	8509571	8510185	E070	32828
chr17	8510192	8510258	E070	33449
chr17	8511807	8512156	E070	35064
chr17	8524133	8524216	E070	47390
chr17	8524389	8524455	E070	47646
chr17	8524612	8524714	E070	47869
chr17	8524959	8525238	E070	48216
chr17	8525281	8525535	E070	48538
chr17	8525650	8525762	E070	48907
chr17	8509571	8510185	E071	32828
chr17	8510192	8510258	E071	33449
chr17	8509571	8510185	E073	32828
chr17	8510192	8510258	E073	33449
chr17	8439335	8439603	E081	-37140
chr17	8509571	8510185	E081	32828
chr17	8510192	8510258	E081	33449
chr17	8524133	8524216	E081	47390
chr17	8524389	8524455	E081	47646
chr17	8524612	8524714	E081	47869
chr17	8524959	8525238	E081	48216
chr17	8439335	8439603	E082	-37140
chr17	8466462	8466611	E082	-10132
chr17	8484195	8485211	E082	7452
chr17	8509571	8510185	E082	32828
chr17	8510192	8510258	E082	33449
chr17	8524133	8524216	E082	47390
chr17	8524389	8524455	E082	47646

rs7208821